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TORREYA 


A MonTHiy JoUuRNAL oF BoTtanicaL Notes anp News 


JOHN TORREY, 1796-1873 


EDITED FOR 
THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


Volume XIV 


NEW YORK 
1914 


OFFICERS FOR 1014 


President 
R. A. HARPER, PH.D. 
Vice-Presidents 
JOHN HENDLEY BARNHART, A.M., M.D. 
HERBERT M. RICHARDS, S.D. 


Secretary and Treasurer 


BERNARD O. DODGE, Ph.D. 
Columbia University, New York City 


Editor 
ALEX. W. EVANS, M.D., PH.D. 


Associate Editors 


JEAN BROADHURST, Pu.D. MARSHALL AVERY HOWE, Pu.D. 
ERNEST D. CLARK, Pu.D. HERBERT M. RICHARDS, S.D. 
fea tARRIS, Pu.D. ARLOW B. STOUT, PH.D. 


NORMAN TAYLOR 


COMMITTEES FOR 1914 
Finance Committee Field Committee 


J. H. Barnuart, Chairman SERENO STETSON, Chairman 
Miss C. C. Haynes 
Budget Committee Program Committee 
J. H. Barnuart, Chairman Mrs. E. G. Britton, Chairman 
N. L. Britton Miss JEAN BROADHURST 
B. O. DopGE C. STUART GAGER 
M. A. Howe F. J. SEAVER 
A. W. Evans 
fe Ei: RUSBY 


Local Flora Committee 
N. L. Britton, Chairman 


Phanerogams: - Cryptogams: 

E. P. BICKNELL Mrs. E. G. BRITTON 
N. L. Britton Puitrep DowELL 
Cc. CURTIS Tracy E. Hazen 

K. K. MAcKkEnzIE M. A. Howe 
NorMAN TAYLOR W. A. MurrRILyi 


Delegate to the Council of the New York Academy of Sciences 
; WILt1AM MANSFIELD 


No. 
No. 
No. 
No. 
No. 
No. 
No. 
No. 
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No 
No 


No. 


2, 
3) 
4, 
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6, 
7) 
8, 
9; 
5 1)5 
Hates 
12, 


1, for January 


February 
March 
April 

May 

June 

July 
August 
September 
October 
November 
December 


DATES OF PUBLICATION 


Pages 1-20 
21-38 
39-54 
539-72 
73-96 
97-114 

T15—132 
133-148 
149-166 
167-200 
201-228 
229-267 


Issued January 27, 
February 9, 
March Lp 
April 8, 
May 14, 
June 8, 
July 7s 
August 12, 


September 18, 


~ October 


27; 


November 27, 


January 


13, 


1914 
1914 
I9I4 
1914 
1914 
1914 
1914 
1914 
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1914 
1914 
IQI5 


ORREYA 


A Monruty Journat or BoranicaL Notes anp News 


EDITED FOR 


THE TORREY BOTANICAL CLUE 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873 
CONTENTS 
Addison Brow :\.F. Fi: Ruspy 2h ached i es pelea ds decdeh lesen Sale ae cota eee: I 
Violets new to southeastern Virginia: H. D. HOUSE.........:0:50.sesseenterece ee retennee 2 
Reviews : 

Two recent Tes on marine algae : MRE Wy asthe oda whe diac cuditaste se lvavemeces 4 
Wilson’s Naturalist in Western China: N. TAvtor..........:- FROIN hs are an 78 
American Breeders’ Magazine: A. B. STOUT....2-..+:..+5++- fp desde cbiepiotec eines epcidems 10 

- Proceedings of the Club nash iy earecee hs Ba Ss De aS OD PDI a a A 11 
pmewattem (hth da cat tue Punk RT RY a sea Mase 18 


PUBLISHED’ FoR THE CLUB 


| Ar 4: Nortu Quzen Street, LANCASTER, Pa. 
By Tue New Era Printing Company. 


[mvered a atthe Post Office at Lancaster, Pa., as reas class matter. j 


THE TORREY BOTANICAL CLUB 


OFFICERS FOR 10913 


President 
EDWARD S. BURGESS, PH-D. 


Vice- Presidents 


JOHN HENDLEY BARNHART, A.M., M.D. 
HERBERT M, RICHARDS, $.D 


Secretary and Treasurer 


BERNARD: O.) DODGE, Ph.D. 
Columbia University, New York City 


Editor 
‘EDWARD | Boe MORRIS* 


Associate Editors 


JEAN BROADHURST, A.M. MARSHALL AVERY HOWE, PH.D 
ERNEST D. CLARK, PH.D. - HERBERT M. RICHARDS, S. D. 
ALEX. W. EVANS, M-D., PH.D. ARLOW'’B. = ROUT: 


NORMAN TAYLOR- 


; Torreya is furnished to subscribers in the United States and 
Canada for one dollar per annum; single copies, fifteen cents. To 
subscribers elsewhere, five shillings, or the equivalent thereof. Postal or 
express money orders and drafts or personal checks on New York City 
banks are accepted in payment, but the rules of the New York Clearing 
House compel the request that ten cents be added to the amount of any 
other local checks that may be sent. Subscriptions are received only 5 
for full volumes, beginning with the January issue. Reprints will. be - 
furnished at cost prices. Subscriptions and remittances should be sent 
to TREASURER, TORREY BOTANICAL CLuB, 41 North Queen St., Lan- 
caster, Pa., or Columbia University, New York City. 


Matter for publication should be addressed to 


NORMAN TAYLOR P 


Brooklyn Botanic Garden : 
* Died 14 September 1913. Sa _ Brooklyn, N. Y._ 


TORREYA 


January, IgIq4. 
Vol. 14 No.1 


ADDISON BROWN 


Judge Addison Brown, a member of this club since the second 
year of its existence and for ten years its president, died on the 
gth of April, 1913, in the eighty-third year of his life. 

Judge Brown’s early studies were pursued under the tuition of 
Benjamin Greenleaf, the mathematician, to whose influence was 
probably due the fondness for astronomy which he always 
displayed. His collegiate course was at Amherst, and later at 
Harvard, where he graduated in 1852. His studies were re- 
markably well balanced and his life was characterized by an 
interest in widely separated fields of investigation. He was a 
competent art critic and a creditable violinist. His legal prepa- 
ration was at the Harvard Law School, from which he gradu- 
ated in 1855. He began the practice of law in New York City in 
the following year. In 1881, he became Judge in the United 
States District Court which position he held until his retire- 
ment, in I9oT. 

Judge Brown’s botanical work, in which we are chiefly in- 
terested, began even before he became a member of this club, 
but was much more active thereafter. His connection with the 
club was most helpful to it, but it is interesting to consider also 
to how great an extent his own work in this field, and his great 
service to botany, were determined by this relation. Almost 
his first active work in local botany was in connection with our 
ballast plants. He preserved his specimens and formed a private 
herbarium, and also accumulated a good working library. 
Although he could not be regarded as a general collector, yet 
he made a number of botanical excursions in distant parts of 
this country and studied portions of the European flora in the 
field. His American travels extended as far as Alaska. 


[No. 12, Vol. 13, of TORREYA, comprising pp. 265-301, was issued 30 December 1913} 


1 


LIBRA 
NEW Y 
BOTAN 

(PakRD 


2 


It is significant of the character of the man that Judge Brown’s 
later work was the more important. His service, in connection 
with Judge Charles P. Daly, in drawing the charter of the 
New York Botanical Garden, was of inestimable value, not only 
to that institution, but to botanical science. He became the 
president of the Garden in r9ro and continued in that position 
until the time of his death. 

He was a subscriber to the endowment fund of the garden to 
the extent of $25,000 and he bequeathed to it property to the 
value of more than $20,000. This bequest is preserved in The 
Addison Brown Fund, the income of which is to be devoted to 
the publication of a magazine with colored illustrations. 

The greatest botanical work in which the Judge participated 
was the writing of Britton and Brown’s Illustrated Flora of the 
Northern United States, Canada and the British Possessions, 
the second edition of which was completed just before his death. 
It should never be forgotten that Judge Brown undertook this 
great work with no expectation that it would ever repay its 
cost. His only anxiety was as to the probable extent of his loss, 
which he hoped would not exceed $25,000; and it is exceptionally 
gratifying, under such circumstances, that the publication proved 
to be financially, as well as scientifically, successful. 

An extended obituary, written by Dr. N. L. Britton, will be 
found in the Journal of the New York Botanical Garden for 


June, 1913. 
H. H. Russy 


VIOLETS NEW TO SOUTHEASTERN VIRGINIA 


By H. D. House 


A single day was spent by the writer in the vicinity of Gilmer- 
ton, Norfolk county, Virginia, in April of 1912, and again in 
April, 1913. The only finds of real interest were violets, abundant 
and easy to find at that season of the year. 


VIOLA SEPTEMLOBA LeConte 
This rare southern species seems well entitled to a position in 
the flora of the northeastern states, having already been twice 


3 


reported from southeastern Virginia. Excellent flowering speci- 
mens were collected by the writer at Gilmerton (No. 4860, 
April 20, I912), concerning a specimen of which Dr. Brainerd 
writes “ . is the most satisfactory one that I have seen from 
Virginia.”’ 

Growing abundantly with the species was found Viola emar- 
gimata (Nutt.) LeConte, and a hybrid between the two, which 
may be designated as 


Viola emarginata X septemloba hyb. nov. 
Plant glabrous at flowering time, the leaves varying from 
deltoid to sagittate, the middle lobe of the blade elongated, the 


Fic. 1. Viola emarginata X septemloba House. (Natural size.) 


4 


lateral lobes very narrow, the basal ones nearly at right angles to 
the middle lobe; summer leaves several-lobed, the middle lobe 
longest and largest; flowers large, pale blue in color (Gilmerton, 
No. 4857, April 20, 1912). 

This hybrid has some resemblance to the hybrid between 
Viola Brittoniana and emarginata, first found in the District of 
Columbia, and figured in Rhodora (pl. 71) in 1906. It lacks, 
however, the stoutness of that plant, and in its more slender 
habit shows its relationship to Viola septemloba. The name 
“ Viola emarginata Xseptemloba’’ has been previously used for a 
hybrid between Viola emarginata and Viola Brittoniana by Ezra 
Brainerd (Rhodora 8: 53. 1906). Dr. Brainerd at that time 
regarded Viola Brittonitana as identical with the more southern 
Viola septemloba, a position from which he has since receded. 


VIOLA VILLOSA Walter 


This southern species has not been previously reported from 
Virginia. It is quite common near Gilmerton on bushy cut-over 
land used as a pasture, the soil being very sandy (No. 5079, 


April 19, 1913). 


REVIEWS 


Two recent works on the marine algae * 


The publication, during the past summer, of Professor Bradley 
Moore Davis’s studies of the marine algae of the Woods Hole 
region marks an important forward step in the study of the 
American algae. In the first part of this work the marine flora 
as a whole and the various associations of species are discussed 
from the biological or ecological point of view. After an in- 
troductory chapter, the author discusses some of the factors 


* Davis, Bradley Moore. A biological survey of the waters of Woods Hole and 
vicinity. Part I. Section II. Botanical. General characteristics of the algal 
vegetation of Buzzards Bay and Vineyard Sound in the vicinity of Woods Hole. 
Bull. Bur. Fisheries 31: 443-544. charts 228-274. 1913; Part II. Section IV. 
A catalogue of the marine flora. Bull. Bur. Fisheries 31: 795-833. 1913. 

Weber-van Bosse, A. Liste des algues du Siboga. 1. Myxophyceae, Chloro- 
phyceae, Phaeophyceae, avec le concours de M. Th. Reinbold. Siboga Expeditie, 
Monographie 59a: 1-186. f. 1-52+ 1. 1-5. S 1913. E. J. Brill, Leiden. 4to. 


5 


affecting the local distribution, such as the nature of the coast 
and of the bottom in deeper water, the tides and tidal currents, 
the effects of ice, depth of water, light, temperature and seasonal 
changes, and salinity of the water. In the third chapter, the 
characteristic algal associations and formations are described 
and analyzed. A chapter of remarkable interest and value 
concerns the algae of Spindle Rocks, a group of ten boulders at 
one of the entrances to the ship channel at Woods Hole. The 
flora of these rocks was under a more or less continuous observa- 
tion during a period of fifteen months and the seasonal variation 
in their flora is shown with great clearness by a series of eight 
charts. It is to be hoped, as the author suggests, that this 
record of interesting results may stimulate others to make 
similar sustained and intensive studies of the flora of other 
limited areas. The first part of Professor Davis’s paper closes 
with an account of the distribution of the marine algae in the 
deeper waters, the flora of certain inshore regions of peculiar 
interest, and with a series of charts illustrating the distribution 
of thirty-eight of the more common and characteristic species of 
the region. 

The catalogue of species, which comprises the second part of 
Davis’s work, includes full details as to distribution and seasonal 
occurrence and cites the specimens and records on which his 
own records are based. The number of species recognized is 
240. The nomenclature of the list is of the current sort. A 
recent reviewer, Mr. F. S. Collins, has commended it as ‘“con- 
forming to the Vienna Rules,’’* which is possibly true of it, to a 
certain degree. However, as Mr. Collins himself has more re- 
cently} hinted, the use of Farlow’s specific name Bornetiana for 
our common Griffithsia is obviously in violation of the Vienna 
Rules. It may be added that the specific name of our handsome 
red alga currently known as Dasya elegans is evidently, under 
the Vienna Rules, pedicellata, the type of the species being a 
specimen from New York sent to the elder Agardh by John 
Torrey. And Phyllitis, under the Vienna Rules and the Brussels 


* Rhodora 15: 152. Ir Au 1913. 
+ Science II. 38: 597. 24 O 1913. 


6 


Amendments, is the legal name for a genus of ferns and as such 
is enjoying wide usage. A careful scrutiny would doubtless 
disclose other less obvious and less well-known violations of the 
Vienna Rules. But these are minor details and, rules or no rules, 
the nomenclature adopted by Professor Davis has the great 
and saving virtue of being readily intelligible. 


Part I of Mme. Dr. A. Weber-van Bosse’s “Liste des algues 
du Siboga,’’ which appeared in September last, includes the 
Myxophyceae [Cyanophyceae], Chlorophyceae, and Phaeophy- 
ceae. It is based chiefly on specimens obtained in the Dutch 
East Indies in 1899-1900 by the scientific expedition under the 
leadership of Professor Max Weber, of the University of Amster- 
dam, the husband of the talented authoress of the “ Liste.”’ 
“Siboga’’ was the name of the Dutch cruiser used on that voyage 
of exploration and the present paper is a part of one of the sixty- 
six memoirs or monographs, for the most part already published, 
in which the scientific results of this expedition are made known. 
A part of the ground covered by the present ‘Liste’ has been 
included in more detail by the general monograph of the genus 
Halimeda by Miss E. S. Barton (Mrs. A. Gepp), constituting 
monograph 60 of the Siboga series, the general monograph* of 
the family Codiaceae by A. and E. S. Gepp, constituting mono- 
graph 62 of the series, and preliminary papers by Mme. Weber- 
van Bosse on Dictyosphaeria, etc. In addition to the material 
secured by the Siboga Expedition, the present ‘“‘Liste’’ takes into 
consideration also specimens “collected by Mme. Weber-van 
Bosse in an earlier visit to the Dutch East Indies (in 1888) and 
certain specimens sent to her by other collectors. The treat- 
ment of the genera Boodlea, Cladophora, Cladophoropsis, Micro- 
dictyon, Rhizoclonium, and Struvea, among the green algae, and 
of Sargassum among the browns, has been contributed by Major 
Th. Reinbold. His parts of the work are published in German, 
while Mme. Weber’s are in French. 

In the treatment of the Myxophyceae, written by Mme. 


* Reviewed in Torreya II: 133-137. Je IgII. 


7 


Weber-van Bosse, one notes the proposal of several new species 
and of one new genus, Herpyzonema, of the family Stigone- 
mataceae. 

The points of contrast between the marine flora of the East 
Indies and that of the West Indies are perhaps nowhere more 
obvious than in the order Siphonales of the Chlorophyceae. Of 
the twenty-five species of the genus Caulerpa, here attributed to 
the Dutch East Indies, ten occur also in the seas of tropical and 
subtropical America. Among the Siphonales of West Indian 
affinities, one notes that Acetabularia caraibica Kiitzing is main- 
tained as a valid species. Through the courtesy of Mme. Weber- 
van Bosse, the present reviewer,* about a dozen years ago, ex- 
amined most of the original materials on which this species was 
based and he expressed the opinion that they could not be satis- 
factorily distinguished from Acetabularia crenulata Lamour., 
described forty years earlier, the type of this also coming from 
the Antilles. This view of A. caraibica has since been adopted 
by Mr. F. S. Collinst and by Dr. Bérgesen,t both of whom have 
enjoyed good opportunities for knowing the West Indian plants 
of this genus. The types of both of the alleged species being 
West Indian, the question of their validity or identity is essen- 
tially a West Indian rather than an East Indian question. Among 
the Siphonales is a new genus Bryobesia Weber-van Bosse, first 
published, however, two or three years earlier, but now illustrated 
and described in more detail. 

Among the Phaeophyceae, Madame Weber uses “‘TJlea (Fr.) 
Nordstedt’”’ for the genus currently known as Phyllitis, which 
name, as remarked in the preceding review, legally belongs to a 
genus of ferns. The name J/ea was first used by Fries for a genus 
of Chlorophyceae and as such is in current usage. Under the 
prevailing European rules of nomenclature, the taking up of Jlea 
for a genus of brown algae may possibly be justifiable, in spite 
of the confusion that it would entail, but the earlier use of Jlea 
in an entirely different sense happily forbids any such boule- 

* Bull. Torrey Club 28: 331-333. I9g0T. : 


+ The green algae of North America 378. 1909. 
t The marine algae of the Danish West Indies 80, 81. 1913. 


8 


versement under the ‘rejection of homonyms’”’ principle of the 
“American Code.’ It seems to the reviewer that Petalonia 
Derb. & Sol. is the right name for the genus of algae commonly 
known as Phyllitis. 

Mesospora Weber-van Bosse is a genus of Ralfsiaceae, pub- 
lished in a preliminary way a few years earlier, but now illus- 
trated and more fully described. 

Major Reinbold, in his treatment of the genus Sargassum, 
recognizes forty-five species, of which three are proposed as new. 
In striking contrast to the genus Caulerpa, the forty-five East 
Indian species of Sargassum appear to include only one, S. baccif- 
erum, that occurs also in the West Indian region. In connection 
with S. bacciferum, the author, by the way, quotes J. Agardh’s 
statement that attached and fructiferous plants of this species 
occur “‘in rupibus extra New Foundland’’—a statement that, 
in all probability, rests upon some sort of error. 

This first part of the “Liste des algues du Siboga”’ is illustrated 
by fifty-two text figures and five handsome plates. The appear- 
ance of the second part of this important work, to include the 
Rhodophyceae, will be awaited with much interest. 

MarsHALL A. HOWE 


Wilson’s A Naturalist in Western China* 


When, in 1859, Asa Gray brought out his now famous paper 
on the relationship of the Japanese flora to that of eastern North 
America, it is doubtful if he realized how completely that idea 
was to be supported by a man who was to explore the interior 
of China more than fifty years later. As we now know, many 
of the plants mentioned by Gray as of Japanese origin were only 
introduced into Japan from China, and his paper must be 
construed today as an attempt to explain the very close relation- 
ship between the flora of eastern North America and eastern 
Asia. 

More than any living botanist, Mr. E. H. Wilson has made it 


* Wilson, E.H. A naturalist in western China with vasculum, camera and gun. 
With an introduction by C. S. Sargent. Vol. I. pp. i-xxxvii+i1-—251. Vol. 2. 
pp. I-229. ror illustrations and map. New York. Doubleday, Page & Co. 1913. 
Price $7.50. 


9 


possible for us to know something of the region in the hinterland 
of China and the Thibetan frontier, his travels and collections 
extending over a period of eleven years. Some idea of the extent 
of his work will be gained by remembering that he has collected 
some 65,000 specimens, comprising about 5,000 species, and sent 
home seeds of over 1,500 different plants. Thousands of these 
are now growing in England at Messrs. Veitch and Son’s and 
an equal, or greater number, mostly woody plants, at the Arnold 
Arboretum in this country. It is difficult to speak with restraint 
of the importance of these additions to our cultivated plants, 
and it is no exaggeration to say that Mr. Wilson’s plants 
form the most important collection ever brought out of China. 
Frequent scattered notices of these plants have appeared in the 
Gardener’s Chronicle and the Botanical Magazine. Many of the 
finer species, horticulturally, are already in the trade, mostly in 
England, but some are to be had here. Of course, the most 
complete collection of the woody plants is at the Arnold Ar- 
boretum, but many private estates have some of them and there 
is a collection of over 400 species now at the Brooklyn Botanic 
Garden. The scientific results of these remarkable expeditions 
have already appeared, in part, as Plantae Wilsonianae, published 
at the Arnold Arboretum. Professor C. S. Sargent has con- 
tributed to the present volume a technical introduction on the 
relationship of the tree flora of China and eastern North America. 
- It would be extraordinary if a traveller and botanist of such 
accomplishments could not make an interesting narrative of his 
journeys in this all but unknown country, and such the present 
work proves to be. It isan intimate and personal account of the 
author’s travels, especially in the vast province of Szechuan and 
the Thibetan frontier, and the wealth of botanical information 
is astounding. Very few of us realize the diversity and richness 
of this temperate flora in western China (it is the richest in the 
world) reaching its greatest profusion at, and westward of a 
point, some thousand miles up the Yangste River (Mr. Wilson 
says Yangste-Kiang is unintelligible to all the Chinese he has 
ever met, and that the name is simply Yangste). No review 
could do adequate justice to the botanical features of Mr. Wilson’s 


10 


book, the information is so much a part of the general text and 
of such varied character. There are, of course, special chapters 
on the medicinal plants, fruits, general economic products, timber — 
trees, agriculture, gardens and gardening, and the tea industry. 

Besides all the interesting data about plants and their products, 
the author has been very much alive to all that was happening 
during his travels, and there is a great deal of very interesting 
narrative in connection with the people of this little known king- 
dom. Particularly the Chino-Thibetan frontier country with 
its all but unknown people has claimed considerable attention. 
Their religions, mode of life and peculiar marriage customs are 
very interestingly dwelt on. There are four chapters devoted 
to sport, in which most of the animals and birds seen during the 
trip are described. A concluding chapter gives, succinctly, the 
causes and probable tendency of the present political unrest in 
China, as they appeal to the author. There are over a hundred 
splendid illustrations accompanying the text, nearly all of which 
were taken by the author on the spot. 

It is not too much to say of these volumes that they should be 
read by all who are interested in botany, by every traveller or 
one who hopes to travel in China, and that for the general reader 
and merchant there is more information in attractive form about 
western China than in any other work that comes readily to mind. 

NORMAN TAYLOR 


The American Breeders’ Magazine* 


The American Breeders’ Magazine for the second quarter, 
1913, announces important changes in the organization and 
administration of the American Breeders’ Association. In regard 
to the character of the magazine published by the association 
for the benefit of its members, the announcement states in part 
as follows: 

“The desire of the new management is, briefly: to retain the 
high standard of scientific accuracy which has made the magazine 
valued in the past, but at the same time to present articles of 


* The price of single copies is $.25. Membership is $2.00 a year. Address all 
communications to American Breeders’ Association, Washington, D. C. 


11 


such a nature, and so well illustrated, that they will interest not 
only those working in the particular field of which the article 
treats, but all who desire to keep informed in an authoritative 
way of progress made in plant and animal breeding and eugenics.” 

The magazine will be issued monthly instead of quarterly as 
hitherto. 

This enlargement and improvement of The American Breeders’ 
Magazine is made possible only by a guarantee fund of $3,000 
annually for three years pledged by members and friends of the 
Association to cover possible deficits. 

It is to be hoped that the increase in membership which the 
~ work and the publications of the association warrant will make 
the use of the guarantee fund unnecessary. 

The number issued for October contains the following articles 
illustrated by eleven full-page plates and one half-page plate: 

Announcement of Reorganization of the Association. 

New Citrous Fruits, by Walter T. Swingle. 

Eugenic Immigration, by Robert DeC. Ward. 

New Plants for Breeders, by David Fairchild. 

Color Inheritance in Swine, by W. W. Smith. 

Publications Received. 

Report of Fourth International Conference on Genetics. 

Association Matters. 

Since the above was written, three further numbers of the 
publication have appeared of which the first two complete volume 
IV. The issue for January, 1914, bears the new title “‘The 
Journal of Heredity,” and announces that the American Breeders’ 
Association is henceforth to be called the American Genetic 
Association. These three issues under the new management 
show marked enlargement and improvement, fully meeting the 


plans announced in the preceding number. 
Ae Bs SOUL 


PROCEEDINGS TOF iH E CLUB 
OCTOBER 29, 1913 


The meeting of October 29, 1913, was held in the laboratory 
of the New York Botanical Garden at 3:30 P.M., Dr. Marshall 
A. Howe acting as chairman. Fifteen persons were present. 


12 


The minutes of the meeting of October 14 were read and 
approved. 

Dr. E. G. Arzberger, Bureau of Plant Industry, Washington, 
D. C., was nominated for membership. 

Dr. H. H. Rusby on behalf of the committee to prepare a 
suitable memorial of Judge Addison Brown submitted a bio- 
graphical sketch which was, on the motion of Professor R. A. 
Harper, referred to the board of editors for publication. 

The resolutions relating to the death of Judge Brown and E. L. 
Morris were ordered engrossed and sent to the families of the 
deceased. 

The first number of the scientific program was a paper on the 
Ambrosiaceae. 

Dr. Rydberg presented some preliminary remarks on the results 
of his investigations of the family Ambrosiaceae of which he is 
preparing a monograph for the North American Flora. His 
work has been -confined to the Ambrosiaceae proper. This 
group is represented in the eastern United States by the genera 
Ambrosia and Xanthium. These two genera were the only ones 
known to Linné when he wrote his Species Plantarum. The 
characters distinguishing the two are the following: 

In Ambrosia the bracts of the staminate heads are united. The 
pistillate head contains usually only one flower and forms a bur 
with a single beak which is 3- or 4-toothed at the apex and very 
little oblique. The bur is armed with a single circle of small 
straight spines. In Xanthiuwm the bracts of the staminate heads 
are distinct. The pistillate head develops into a bur with nu- 
merous hooked spines and two beaks which are very oblique at 
the mouth and have only 2 lobes, of which the outer one is much 
longer and usually hooked. The younger Linnaeus described 
in the Supplementum Xanthium fruticosum, which disagrees 
with the whole genus in having the bracts of the staminate heads 
united as in Ambrosia. 

Medicus claimed that the older Linnaeus had included this 
species in Ambrosia, which statement has been impossible to 
verify. Medicus in Act. Acad. Theod. Palat. 3:'247. 1775 dis- 
cusses this species, still including it in Ambrosia, but suggests 


13 


that it may constitute a distinct genus. In 1889, in Philosophia 
Botanica he actually proposed it as a genus, Gaertneria. Unfor- 
tunately there is a Gaertnera of Schreber of the same year. In 
1793, Cavanilles described the new genus Franseria. Most 
authors have regarded Gaertneria of Medicus and Franseria of 
Cavanilles the same. The genus has been known mostly under 
the latter name. O. Kuntze was the first one in later years who 
took up the older name Gaertneria, but he dates it from 1775 the 
year when Medicus first discussed the species, but as he did not 
propose a new name for it, but still retained the species in Am- 
brosia, this cannot be regarded as publication; and Gaerineria 
might be antedated by Gaertnera Schreber. However, a new 
question arises. 

The only character separating Xanthium and Franseria is the 
distinct bracts of the staminate heads in the former and the united 
ones in the latter. In one species of Franseria the bracts are 
only united at the base and this character might not be generic. 
In other respects the original Franseria is very closely related to 
Xanthium, having many numerous and hooked prickles and 2-4 
beaks on the fruit, of the character of those in Xanthium, while 
the most species that have been included in Franseria are closely 
related to Ambrosia. As stated before, Ambrosia has only one 
beak that is scarcely oblique at the apex and usually 3-4-toothed. 
This character is also found in two North American species of 
Franseria, but all the other species have 2-toothed, very oblique 
beaks as in Xanthium. Some have one beak, some two or even 
as many as six or seven. The question is whether the number of 
beaks, the number and structure of the spines are not just as 
good generic characters as the number of series of spines and the 
union or non-union of the bracts of the staminate heads. If such 
combinations are made the genus Franseria should be divided into 
several genera. Such species as Franseria acanthicarpa, tenu- 
folia and bipinnatifida differ very little from Ambrosia, the 
distinction being in consisting only of 2-4 series of spines instead 
of single ones and an oblique 2-toothed beak. The general 
habit is that of Ambrosia and the staminate heads essentially 
identical. Such species as Franseria discolor and tomentosa are 


14 


also very close to Ambrosia, but the beaks are 2 or more. The 
number of beaks corresponds also to the number of cavities in 
the bur. Each cavity and beak contains usually only one pistil 
but sometimes two. These species are closely related to the 
original Gaertneria. In all these species the spines are rather 
few, seldom 30, and either short and without any hooks at the 
end, or else more or less flattened or channeled on the upper side. 
The original species of Franseria on the contrary has numerous 
spines and numerous series, the number of spines being over 100. 
They are long and slender and hooked at the end, and the whole 
fruit in structure agreeing with Xanthium. 

The only one who has tried to make segregates in the genus is 
Delpino, who proposed the genera Xanthidium, Hemixanthidium 
and Hemiambrosia, but his arrangements cannot be followed, 
because he included in Xanthidiwm the original supposed Fran- 
seria and Gaertneria and applied the name Franseria to the I- 
beaked species most closely related to Ambrosia. Besides the 
name Xanthidium is preoccupied. _ Hemixanthidium was proposed 
on a species which Delpino claimed had two kinds of pistillate 
heads, the one kind described as the ordinary one, the other form 
as found occasionally but as evidently caused by some disease. 
His Hemiambrosia is based on the species which would be included 
in Ambrosia. 

There are two species of Franseria, however, that are very 
peculiar in their structure, namely, F. eriocentra and F. Bryantt. 
Both have a single beak which is scarcely oblique and with 
several teeth. 

The former has only one pistil, but the spines are in several 
series and the plant is of quite different habit, otherwise the 
plants could be included in Ambrosia. The most peculiar of all 
is F. Bryantt, which also has a single beak, and the spines are 
practically in a single series. According to these characters the 
plant should be included in Ambrosia, but the bur contains 
several pistils and is several-celled, although the beak is single 
and the spines are enormously elongated, sometimes 2-3 cm. 
long. If none of the other species of Franseria are regarded as 
generic types, this one should. It is more distinct from Fran- 


15 


seria than from Ambrosia, but could not be included in the latter 
genus. 

Where the generic line should be drawn is hard to tell and 
Dr. Rydberg was not prepared to give his final conclusions. It 
is evident, however, that the treatment hitherto followed is not 
satisfactory. Some of the species of Franseria could easily be 
included in Ambrosia by modifying the latter genus a little. 
Other species are on the other hand so closely related to Xanthium 
that it is hard to draw any line, except the united bracts and the 
staminate heads. It would be better to segregate the genus 
_ Franseria into several than to leave it as it is, but where and how 
to draw the generic line is hard to tell. 

There is another genus of the same group, namely, Hymenoclea. 
The structure of the pistillate head is essentially that of Ambrosia, 
except that small spines of that genus have been replaced by 
broad and thin wings. The beak is essentially of the same struc- 
ture. In one species the wings are in a single series, but in the 
other species there are some scattered wings below. In this 
respect, the species stand to each other in the same relationship 
as the genera Franseria and Ambrosia, but none of the species 
have the beak of Franseria. There will be no good reason for 
segregating them into several genera on account of the number of 
series of appendages. 

Why should the number of series be regarded as a good char- 
acter in separating Franseria and Ambrosia? And then the 
question arises, if all four genera in reality could not be regarded 
as one. There seems to be no reason why they should not if 
Franseria is left as it 1s. 

Dr. Britton announced the approaching completion of Mr. 
Norman Taylor’s studies on the local flora within 100 miles of 
New York City, which have extended over several years, and 
also the authorization of the publication of the results of this 
work by the scientific directors of the New York Botanical 
Garden. The greater portion of the investigation was accom- 
plished during the period while Mr. Taylor was an officer of the 
New York Botanical Garden, and has been completed during his 
association with the Brooklyn Botanic Garden. Dr. Britton 


16 


remarked on the preceding ctalogues of the local flora, including 
the list prepared by Dr. Torrey, Dr. Eddy, and Mr. Knevals, 
published by the Lyceum of Natural History in 1819, the list 
prepared by Mr. Leggett and his associates, published in Volumes 
1-6 of Bulletin, 1870-1876, and the catalogue of 1888, prepared 
by himself with the aid of Mr. Stearns and Mr. Poggenburg. 
Mr. Taylor’s work is much more elaborate than any of the pre- 
ceding catalogues, as it contains keys for the rapid determination 
of species, detailed citations of distribution, and of habitat, 
together with statements of distribution by geological formations, 
by altitude, and with relation to temperature and the length of 
the growing season. 

Mr. Otto Kunkel spoke of collecting rusts in the Adirondacks. 
Dr. R. M. Harper gave a brief description of certain floral 
features of northern Michigan. An abstract follows: 

The biological station of the University of Michigan is located 
in the wilderness on the shore of Douglas Lake, about 17 miles 
south of the Straits of Mackinac. The lake covers seven square 
miles, and has a varied and interesting flora along its shores. 
The surrounding country is very sandy, and was originally 
covered mostly with white pine forests, which were cut off about 
thirty years ago, and have not reproduced themselves to any 
considerable extent since, on account of too frequent fires. 
There are small areas of hardwood forest, in nearly primeval 
condition, and many swamps full of conifers of the traditional or 
conventional narrow conical form, familiar in all parts of the 
northern hemisphere where the snowfall is heavy. The abun- 
dance of fleshy fruits in that neighborhood, which is near the 
southern edge of the boreal conifer region, is noteworthy. They 
occur in many different families, even including the Cyperaceae. 


Adjournment followed. 
B. O. DoncE, 


Secretary 
NOVEMBER II, I913 
The meeting of November I1, 1913, was held at the American 
Museum of Natural History at 8:15. President Burgess presided. 
Twenty-four persons were present. 


Ng 


The minutes of October 29 were read and approved. Dr. O. E. 
White, Brooklyn Botanic Garden, Brooklyn, N. Y., was nomi- 
nated for membership. 

The scientific program consisted of an illustrated address on 
“Spore Formation in the Slime Moulds,” by Prof. R. A. Harper. 

Adjournment followed. 

MiIcHAEL LEVINE, 
Secretary pro tem. 
NOVEMBER 26, 1913 
_ The meeting of November 26, 1913, was held in the laboratory 
of the New York Botanical Garden at 3:30 P.M. with Vice- 
president Barnhart presiding. Twelve persons were present. 

The minutes of November 11 were read and approved. 

Dr. G. Clyde Fisher, American Museum of Natural History, 
New York City, was nominated for membership. 

On the motion of Dr. Murrill, the secretary was instructed to 
accept the terms proposed by the De Felice Company in con- 
nection with the engrossing of the resolution relating to the death 
of Judge Addison Brown and E. L. Morris, such engrossing having 
been authorized at the last meeting. 

Dr. E. G. Arzberger, Dr. O. E. White and Dr. G. Clyde Fisher 
were then elected to membership in the Club. 

Dr. Murrill exhibited specimens of a species of Phellorina 
collected near Laredo, Texas, by Dr. J. N. Rose in October, 1913. 
He pointed out the relationship existing between this genus and 
Podaxon and also spoke briefly of the family Podaxaceae, com- 
prising ‘peculiar, stalked, puffball-like fungi inhabiting desert 
places. 

Mrs. E. G. Britton followed with the announced paper on 
‘“Mosses of the Virgin Islands and Central America.”’ 

Mrs. Britton showed a collection of mosses made in the Danish 
West Indies and the Virgin Islands during the month of Febru- 
ary, 1913, and also a small collection from St. Kitt’s. She read 
an account of the work done by J. Breutel in 1841 (quoted from 
Urban’s Symbolae) on these islands and exhibited a collection of 
specimens preserved in the Mitten Herbarium, which included 
six species from St. Thomas and St. Jan, and six from St. Kitt’s, 


18 


including Hymenostomum Breutelii (C. M.) Broth. which is 
common on St. Thomas. The collections of this year included 
75 specimens, representing 26 species and 19 genera of mosses, 
including 2 new species, one a small Phascum, collected on road- 
side banks, near Charlotte Amalia and an undescribed species of 
Hyophila from the Island of St. Jan collected by Dr. Britton and 
Dr. Shafer. 

Mrs. Britton also read by title, for publication in the Bulletin, 
a report on some collections of Central American mosses sent 
for determination from the National Museum including specimens 
from Guatemala and Costa Rica, including also some specimens 
from Honduras collected for the New York Botanical Garden by 
Mr. Percy Wilson. These included 54 species representing 34 
genera, with descriptions of a new species of Macromitrium and 
a new genus Isodrepanium raised from subgeneric rank to include 
two synonyms, with illustrations and specimens collected in 
Jamaica, Central America and South America. 

Mr. Taylor gave some account of the flowering plants collected 
by Mr. Robert Cushman Murphy on the island of South Georgia 
in the Antarctic regions. Specimens were exhibited, and one or 
two illustrations also, from the work of Dr. Carl Skottsberg. 


Adjournment followed. 
B. O. DonceE, 


Secretary 
NEWS ITEMS 


At the annual meeting of the New York Academy of Sciences 
held December fifteenth, the following botanists ‘were elected 
fellows of the academy: Oakes Ames, R. A. Harper, Wm. Mans- 
field, W. A. Murrill and Norman Taylor. At the same meeting 
Dr. N. L. Britton presented the name of Sir David Prain, 
Lieut.-Col., director of the Royal Botanic Gardens, Kew, for 
election as an honorary member of the academy. Dr. M. A. 
Howe was elected a councilor for 1914-1916. 


Professor F. L. Stevens; of Mayaguez, Porto Rico, has accepted 
the position of professor of plant pathology at the University of 
Mlinois. The appointment becomes effective February 1, and 
thereafter Professor Stevens’s address will be Urbana, III. 


19 


Rev. Reuben Denton Nevius, D.D., died at Tacoma, Wash- 
ington, December 14, 1913. He was born at Ovid, New York, 
November 27, 1827, and was a graduate of Union College of the 
class of 1849. He was a Protestant Episcopal clergyman and 
missionary, and, it is said, had been instrumental in establishing 
more than thirty churches and chapels in the Pacific Northwest. 
As a botanist he was known for his work as a collector in Alabama, 
Oregon, Washington, and Idaho. Asa Gray dedicated to him 
the handsome rosaceous shrub Neviusia alabamensis, which is 
known only from two localities in Alabama. Chenactis Nevii, 
Mnium Nevu, Racomitrium Nevii, Sedum Nevii, and perhaps 
other species commemorate his botanical interests. Dr. Nevius 
is reputed to have possessed the best collection of diatoms in the 
Northwest. 


P. B. Kennedy, Ph.D.,’99, Cornell, professor of botany, 
horticulture and forestry in University of Nevada College and 
Experiment Station, has accepted a position with the University 
of California as assistant professor of agronomy, beginning 
January I, I914. 


Mrs. Agnes Chase, assistant in systematic agrostology, U. S. 
Department of Agriculture, has returned from Porto Rico where 
she has been collecting and studying grasses for about two 
months. Of the 123 species of grasses known from the island 
she obtained all but three, and about 40 additional species. 
Arthrostylidium sarmentosum Pilger, a climbing bamboo, known 
only in the sterile condition, was obtained in flower. 


Dr. Arthur Hollick, curator of paleobotany at the New York 
Botanical Garden for many years, has resigned to accept the 
position of curator-in-chief, of the Museum of the Staten Island 
Association of Arts and Sciences, vacated by the resignation of 


Mire G1 Pollard: 


We regret to record the death of Mr. C. B. Robinson at the 
island of Amboina announced in the daily papers at Christmas. 
Details are as yet lacking and the date of his death is unknown. 
He was collecting there for the Philippine Bureau of Science. 


20 


According to the Evening Post, George W. Hess, of the District 
of Columbia, has been appointed Superintendent of the National 
Botanic Garden to succeed C. Leslie Reynolds, who died recently. 
Mr. Hess is forty-nine years old, and has been growing flowers 
and trees since he was sixteen. For the last few years he has 
resided in the South. Atarecent civil service examination he got 
a rating of 100 per cent. on the growing of foreign plants, and 98 
per cent. on general gardening. 


At the annual meeting of the Club held Tuesday, January 13. 
the following officers were elected for the coming year: Presi- 
dent, R. A. Harper; Vice-Presidents, J. H. Barnhart and H. M. 
Richards: Secretary and Treasurer, B. O. Dodge; Editor, A. W. 
Evans and the following Associate Editors, Jean Broadhurst, E. 
DD: Clark, J.-A. Harris, M.. A. Howe, H. M. Richards:cA] Be 
Stout, and Norman Taylor. Dr. William Mansfield was elected 
delegate to the council of the New York Academy of Sciences. 


: ® 
The Torrey Botanical Club 
Contributors of accepted articles and reviews who wish six 
- gratuitous copies of the number of TorREyAin which their papers 
appear, will kindly notify the editor when returning proof. 
~ Reprints should be ordered, when galley proof is returned 
to the editor. The New Era: Printing Co., 41 North Queen 


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2pp 4pp —s- &pp 12pp 16pp 20pp 

25 copies $.75 $1.05 $1.30 $1.80 $2.20 $2.50 
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- Plates for reprints, 40 cents each per 100. 


The following Committees have been appointed for 1913 


Finance Committee __ *- Bield Committee 
J. I. Kane, Chairinant SERENO. STETSON, Chazriman 
RoperT A. Harper ; 
Budget Committee ‘ Program Committee 
-jJ. H. Barnuart, Chairman Mrs. E. G. Britton, Chairman 
N: L. Britton : Miss JEAN BROADHURST 
ays O. DopdGE € Sruart Gacer 5° 
M. A. Howe F, J. SEAVER 
E. L: Morris 
H. H.-Ruspy 


Local Flora Committee 
N..L. Britton, Chairinan 


Phanerogams: Cryptogams: 
UES PY BICKNEEL tr Mrs. E. G. Britron 
N. L. Britton Puitie DOWELL 

C2C Curris to Tracy Es HAZEN 

K. K. Mackenziz > 2M. A? HowE 

‘E. L. Morris W. A. Murri_i 


NorMAN TAYLOR 
epee se to the Council of the New York Academy of Sciences 


WILLIAM ees 
* Died September 14, 1913. 
{ Died February 1, 1913. 


OTHER PUBLICATIONS 


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Vol. 14 ‘ : February, 1914 No. 2 


“TORREYA 


A Monruty Journar oF Boranicat Notes anp News 


EDITED FOR 


THE. TORREY BOTANICAL CLUB 


BY 
NORMAN TAYLOR 
JOHN TORREY, 1796-1873 
CONTENTS 
_ Two Additions to the flora of Louisiana: P. C. STaNDLEY......--.--.-. SE ESE, 21 
Central American mosses: E. G. BriTTon and RS. WILLIAMS)... eeeteeeeee eee 24 — 
‘Shorter Notes: 
Winter changes in weeping willow : JEAN BROADHURST «2-..-:01..2-505000+ ene 3r- 
» A new form of Pyrola bracteata: J. K. HENRY ..-.:eeeeeccs: pes es eee 32 
“i Current Literature and Notes........ CA mee GCN apo Px Rao, Bos ene aa ae BUA 132 


News Items ......2..ee.tee ee eee eee ete eats DBS Sa EAROA P na Pee ER AEE 37 


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THE TORREY BOTANICAL CLUB 


OFFICERS FOR 1914 


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R. A. HARPER, Pu.D. 
Vice-Presidents 
JOHN HENDLEY BARNHART, A.M., M.D. 
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Columbia University, New York City 


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TORREYA 


February, Ig14. 
Vol. 14 No. 2 


TWO ADDITIONS TO THE FLORA OF LOUISIANA 


By PauL C. STANDLEY* 


Recently two plants were sent for determination to the U. S. 
National Herbarium by Mr. E. C. Wurzlow, of Houma, Louis- 
iana. Upon attempting to name them it was found that neither 
was included in Small’s Flora of the Southeastern United States, 
although, from what Mr. Wurzlow writes concerning them, both 
deserve a place in any flora of Louisiana, being well established 
and so large and showy as to be at once noticed by any botanical 
collector. One of them, a member of the Acanthaceae, was sent 
for identification te Dr. G. Lindau, of Berlin, well known as an 
authority upon this group, who reports that it is the plant 
described from Mexico by Nees as Cryphiacanthus angustifolius. 
Since both plants received from Mr. Wurzlow are of considerable 
interest it seems desirable to make some permanent record of 
them. The data given below concerning disiribution and growth 
in Louisiana are from copious notes kindly furnished by the 
collector. 


RUELLIA SPECTABILIS Britton 


Cryphtacanthus angustifolius Nees in DC. Prodr. 11: 199. 1847, 
not Ruellia angustifolia Sw. 1788. 

Ruellia Tweediana Hemsl. Biol. Centr. Amer. Bot. 2: 508. 
1882, not Griseb. 

Ruellia spectabilis Britton, Ann. N. Y. Acad. Sci. 7: 192. 1893. 
Nees based his description upon two specimens, the first from 

Jalapa, Mexico, collected by Galeotti, the second from Entre 

Rios, Argentina, collected by Tweedie. Grisebach, finding 

that the two collections represented distinct species, named the 
* Published by permission of the Secretary of the Smithsonian Institution 


[No. 1, Vol. 14 of TorREYA, comprising pp. I-20, was issued 27 January, 1914.] 
PAA 


GARDE 


22 


Argentina plant Ruellia Tweediana.* The specific name angusti- 
folius being preoccupied under Ruellia, Dr. Britton in 1893 
renamed Nees’s species Ruellia spectabilis, an appropriate name 
since it is one of the most showy members of the genus. 

Hemsley in the Biologia Centrali-Americana reports the plant 
from Mexico as Ruellia Tweediana Griseb.?, citing only the 
original collection by Galeotti. Dr. Lindau writes that few 
specimens exist in European herbaria. In the U. S. National 
Herbarium there is a single collection apparently referable here, 
gathered by C. G. Pringle (no. 5043) on river ledges near Micos, 
San Luis Potosi, Mexico, distributed as Ruellia Tweediana. 

About Houma, Louisiana, this plant appears to be an escape 
from cultivation. Mr. Wurzlow states that in his early boy- 
hood his father imported a number of plants for cultivation 
and that this is probably one of them. It is now more or less 
common in Terre Bonne Parish, growing in cultivated and waste 
ground, often along ditches, seeming to prefer moist or wet places 
where it spreads rapidly from seed. It is also found within 
enclosures but grows without any care, the plants being so attrac- 
tive with their handsome flowers and showing so little tendency 
to become troublesome weeds, that they are not looked upon 
as intruders. They grow to a height of 3 or 4 feet, sending up 
new stems every year from the rootstocks and flowering from 
July to October. The stems, branches of the inflorescence, and 
veins of the leaves are more or less tinged with purple. The 
corollas are lilac or purple and very showy, being about 5 cm. 
long. The leaves are narrow for the genus, being only 7 to Io 
mm. wide, and 20 cm. long. ; | 

The occurrence of Ruellia spectabilis in Louisiana is of parti- 
cular interest because it must be rare in its native region, other- 
wise so conspicuous a plant could not have been overlooked by 
collectors. It does not seem to be frequent in cultivation for 
it is seldom mentioned in literature. 


S1PHONANTHUS INDICA L. 
Siphonanthus indica L. Sp. Pl. 109. 1753. 
Ovieda mitis L. Sp. Pl. ed. 2. 889. 1762. 
* Symb. Fl. Arg. 259. 1879. 


23 


Clerodendrum Siphonanthus R. Br. in Ait. Hort. Kew. ed. 2. 4: 

Oy TSr2: 

Clerodendrum indicum Kuntze, Rev. Gen. Pl. 2: 506. 1891. 

This is well known under the name Clerodendrum Sipho- 

nanthus, but after a study of its synonymy it is evident that the 
proper designation is Siphonanthus indica. In the Species 
Plantarum Linnaeus published three genera that have usually 
been combined as one, Clerodendrum. ‘These are Siphonanthus 
on page 109, and Ovieda and Clerodendrum* on page 637, Ovieda 
having precedence on the page. 
A single species is published under each genus, these being 
Siphonanthus indica, a well known plant of India, Ovieda spinosa 
(Clerodendrum spinosum Spreng.), common in the West Indies, 
and Clerodendrum infortunata, also from India. The first two 
plants are generally placed in the section Siphonanthus Schauerf of 
the genus Clerodendrum. The group of species included in this 
section has some claim to rank as a genus, because of differences 
in the form of the corolla from that of typical Clerodendrum, but 
apparently recent authors have not separated it. It is apparent, 
however, that if all the species commonly referred to Cleroden- 
drum are to be combined in a single genus this must bear the 
name Siphonanthus. The writer has not attempted to deter- 
mine the desirability of separating Siphonanthus and Cleroden- 
drum, since there can be no question, under the American code 
of botanical nomenclature, as to the proper name for the plant 
discussed here. 

Linnaeus based his Szphonanthus indica upon the name Siphon- 
anthemum, applied by the Russian botanist Ammann in 1739 
to an Indian plant. The species is said to be common in India 
and Java. In the U. S. National Herbarium there are Old 
World specimens from Bengal and Upper Burma. It is common 
in cultivation, especially in tropical and subtropical regions. 
Bailey’s Cyclopedia of Horticulture gives the common name as 
““Turks’ turban”’ and states that the plant is “hardy in Florida.”’ 
In the West Indies it has escaped from cultivation and become 

* This name is usually given as Clerodendron, but Linnaeus always writes it 


Clerodendrum. 
7 In DC. Prodr. 11: 670. 1847. 


24 


established. Specimens are at hand which show that it occurs 
in Guadeloupe, Martinique, and St. Croix, while Grisebach* 
states that it is naturalized in St. Kitts, Trinidad, and Guiana. 

Langlois in his Catalogue Provisoire de Plantes de la Basse- 
Louisianej mentions a ‘‘ Clerodendron sipho’’ as introduced at 
Point a la Hache, on the lower Mississippi. This is doubtless 
the plant that has now become so well established in southern 
Louisiana. Mr. Wurzlow writes that he has observed it for 
many years, not only in Terre Bonne Parish, where it is very 
common, but in other parishes of the southern part of the state. 
It grows along roadsides, ditch banks, and fencerows, and in 
cultivated ground to such an extent that it is regarded as a weed, 
It is distributed by seed, but after the plants are established 
they spread rapidly by rootstocks, forming large patches. Re- 
peated cutting or destruction of the tops does not destroy it 
when it invades cultivated fields. Although frequently seen 
in neglected places about dwellings it is not known to be in 
cultivation. 

Prof. R. S. Cocks, of Tulane University, writes that so far 
as he knows the plant was first collected in 1884 by Dr. Joor near 
Baton Rouge. He further states that it occurs abundantly in 
the vicinity of New Orleans and occurs more or less commonly 


throughout southeastern Louisiana, especially in alluvial soils. 
U. S. NATIONAL MusSEUM 
WASHINGTON, D. C. 


CENTRAL AMERICAN MOSSES 


By ELIZABETH GERTRUDE BRITTON AND ROBERT STATHAM WILLIAMS 


1. Campylopus filifolius (Hornsch.) Mitt. 
Guatemala: Alta Verapaz, 3330a, Maxon and Hay, 1904; 
Alta Verapaz, 29, Cook and Doyle, 1905. 
Costa Rica: Cartago, 506, Maxon, 1906. 
2. Campylopus subleucogaster (C. Miill.) Jaeger. 
Guatemala: Cubilquitz, 6652, H. von Turckheim, 1892. 
Costa Rica: Vicinity of Coliblanco, 264, Maxon, 1906. 


* RI, Brit. W. Ind. 500. 1864. 
Tp.1I5. 1887. 


25 


3. Leucobryum antillarum Sch. 

Costa Rica: Coliblanco, 227a, Maxon, 1906. 

4. Syrrhopodon incompletus Schwegr. 
Syrrhopodon Hobsont Hook. & Grev. 
Syrrhopodon decolorans C. Miill. 
Syrrhopodon Mohrianum C. Mill. 
Syrrhopodon Sartori C. Miill. 

Mexico: Liebman, Sartorius, etc. 

Guatemala: Bernouille and Cario, Rio Pollochico, 3087, Maxon 

and Hay, 1904. 

Honduras: Rio Platano, 690, Wilson,. 1903. 

5. Hyophila reflexifolia C. Miill. 

Guatemala: Alta Verapaz, 411, Cook and Griggs, 1902. 
6. Macromitrium Tonduzit Ren. and Card. 

Costa Rica: La Palma, 481, Maxon, 1906. 
7. Macromitrium palmense R. S. Williams sp. nov. 

Pseudoautoicous: growing in deep tufts, the primary stems 
creeping, bare, the secondary erect, branching, without radicles, 
5 or 6 cm. high; leaves densely imbricate, spreading, crispate in 
upper part; stem leaves 5 mm. long, linear-lanceolate, carinate, 
serrulate about one half down, smooth throughout or with a few 
low papillae on upper surface toward the base; excurrent costa 
slightly denticulate; leaf cells below long and narrow, the median 
in rows, about 6u wide by 10 to 12 long, with furrows between, 
or sometimes scarcely elongate in less distinct rows, the upper 
elongate, not in rows; perichaetial leaves a little shorter than 
stem leaves with longer cells above and more abruptly narrowed 
to the denticulate, excurrent costa; seta smooth, 1.5 to 2.5 cm. 
high; capsule smooth or nearly so, globose-pyriform, about 1.5 
mm. high with stomata in several rows near base; lid not seen; 
peristome double, the outer of reddish-brown, densely papillose 
teeth, divided scarcely one half down, the inner of about the 
same height, a little paler, more or less irregularly divided; 
calyptra without hairs, slightly rough at apex; spores slightly 
rough, up to 35u in diameter. 

In habit much like M. subcirrhosum but with median leaf cells 
very different, leaf base scarcely papillose and costa distinctly 
excurrent. 

HABITAT: On tree trunk on open moist slopes. 

TYPE LocaLity: La Palma, Costa Rica, 480, Maxon, May 6, 
1906. 


26 


8. Macromitrium cirrhosum (Hedw.) Brid. 
Guatemala: Alta Verapaz, 3125, Maxon and Hay, 1905. 
9. Pohlia falcata (Besch.) Broth. 
Guatemala: Volcan de Agua, 3706, Maxon and Hay, 1905. 
10. Acidodontium megalocarpum (Hook.) Ren. and Card. 
Guatemala: Alta Verapaz, 430, Cook and Griggs, 1902; .3290, 
Maxon and Hay, 1905. 
11. Rhizogonium spiniforme (L.) Bruch. 
Guatemala: Alta Verapaz, 843, Cook and Griggs, 1902. 
Costa Rica: Coliblanco, 263, Cartago, 499, Maxon, 1906. 
12. Philonotis sphaerocarpa (Sw.) Brid. 
Honduras: 487, Percy Wilson, 1903. 
13. Philonotis uncinata gracilenta (Hpe.) Dismier. 
Guatemala: San Felipe, 3550, Maxon and Hay, 1905. 
14. Polytrichum antiularum Rich. 
Polytrichum vernicosum Paris. 
Guatemala: Baja Verapaz, 6930, von Turckheim, 1906. 
Costa Rica: Coliblanco, 231, 337, La Palma, 423, Maxon, 1906. 
15. Orthostichidium pentagonum (Hpe. & Ltz.) C. Miill. 
Costa Rica: San José, 164, Cook and Doyle, 1903. 
16. Squamidium macrocarpum (Spruce) Broth. 
Costa Rica: Santiago, 82, Maxon, 1906. 
17. Papillaria nigrescens (Sw.) Jaeg. 
Guatemala: Chilion, Bernouille, 1867. 
Costa Rica: San José, 146, Cook and Doyle, 1903; 146, Maxon, 
1906. 
18. Phyllogonium viscosum (P. Beauv.) Mitt. 
Costa Rica: San José, E. S. Hyde, 1888. 
Coliblanco, 236, Maxon, 1906. 
19. Phyllogonium fulgens gracile Ren. & Card. 
Costa Rica: San José, E. S. Hyde, 1888; Santiago, Aman 
Breues, I90OI. 
20. Neckera Ehrenbergu C. Miill. 
Guatemala: Volcan de Agua, 3716, Maxon and Hay, 1905. 
21. Porotrichum sp. ? (young plants too small to name). 
Costa Rica: La Palma, 384a, Maxon, 1906. 
22. Entodon stenocarpus (Br. & Sch.) Jaeg. 
Costa Rica: San José, 165, Cook and Doyle, 1903. 


27 


23. Fabronia flavinervis C. Mill. 

Guatemala: San Felipe, 3508, 3510a, Maxon and Hay, 1905. 
24. Fabronia polycarpa Hook. 

Panama: Between Salanca and Chiquin, O. F. Cook, 1905. 
25. Pilotrichum bipinnatum (Schwer.) Brid. 

Guatemala: Alta Verapaz, 500, Cook and Griggs, 1902. 
26. Isodrepanium (Mitt.) E. G. Britton gen. nov. Fig. 1. 


Fic. 1. Isodvepanium lentulum (Wils.) E. G. Britton. 


Lepidopilum Sect. Isodrepanium Mitt. Journ. Linn. Soc. 12: 369. 
1869. 
Among our Jamaica collections we have fine specimens of a 
moss which we had difficulty in referring to any genus known 
to us from the West Indies and this difficulty still remains for 


28 


according to Brotherus* it cannot be a Homalia because the 
leaves have porose cells and although they are ecostate they are 
not entire and hence do not fit with Euhomalia or Spathularia. 
According to Mitten this has been described as a subgenus of 
Lepidopilum with one species L. membranaceum (C. M.) Mitt. 
charaeterized by its equally falcate, scythe or scimitar-shaped 
leaves. There is but one species, but it is listed in three genera 
in Paris Index, as Homalia, Lepidopilum and Neckera. The 
identity of these species has been determined by consulting type 
material of each and as the fruit has not been described we give 
the following characters: 


Iscdrepanium (Mitt.) E. G. Britton gen. nov. 


Plants occasionally a foot long, pendent on trees. Stems 
slender, regularly pinnate or bipinnate, branches I-14 cm. long. 
Leaves glossy, imbricate, falcate, acuminate, serrate, ecostate; 
cells porose. Dioicous. Seta 4 cm. long, slender, flexuose; 
capsule nodding-ovoid; peristome double, without cilia. 

Type species: Homalia lentula Wils. 


Isodrepanium lentulum (Wils.) E. G. Britton new combination. 


Homalia lentula Wils. Ann. Mag. Nat. Hist. 20: 379. 1847. 

Hookeria membranacea C. M. Syn. Musc. 2: 200. 1851. 

Lepidopilum membranaceum Mitt. Journ. Linn. Soc. 12: 369. 
1869. 

Neckera falcifolia R. & C. Bull. Soc. Roy. Bot. Belg. 32: 184. 
1893. 

Homalia membranacea C. M. Hedwigia 37: 266. 1808. 

Neckera lentula Broth. in E. & P.-Pfl. 13: 842. 1906. 


Stems pendent, irregularly branched, reaching a maximum of 
30 cm. in length with branches pinnate or bipinnate, often IO-15; 
cm. long; leaves glossy green, crowded, flexuose, I.5 mm. long, 
falcate-acuminate, ecostate; apex recurved; margins unequally 
and finely serrate; base oblique, unequal, slightly auriculate on 
one side, basal cells yellow, enlarged, all femur-shaped and 
porose, with thick walls. Perichaetial leaves longer pointed, 
almost entire. Dioicous. Seta 4 cm. long, slender, flexuose, 
red; capsule 2-3 mm. long, ovoid, horizontal; peristome double, 
yellow; teeth trabeculate, with narrow projecting lamellae, 


* KE. and P. Pflanzenfam. fasc. 226: 847. 1906. 


29 


slender and papillose at apex; endostome paler, smooth, seg- 
ments carinate and perforate, cilia none; walls thickened, cells 
small, irregularly hexagonal; spores smooth, 16-18 pw. Lid and 
calyptra not seen. 


TYPE LOCALITY: Port Royal, Jamaica. ‘‘Mc Nab.” 

DisTRIBUTION: High Mountains of Jamaica, Morce’s Gap, 
John Crow Peak, New Haven Gap and Sir John and Summit, 
St. Catharine’s Peak; Cuba, Sierra Maestra and Mt. Torquino; 
Porto Rico, Luquillo Mts.; St. Vincent, H. H. Smith; Barbadoes, 
Parker; Trinidad, Criiger. Guatemala, Alta Vera Paz, H. von 
-Turckheim 1149, Cook and Griggs 512, with fruit. Costa Rica, 
Pittier 9642; New Granada and Mt. Abitana, Andes of Quito, 
Spruce 740. 

Funck and Schlim, 370 from Caracas, Venezuela, is not this 
species but a true Homalia. 

Homalia glabella (Sw.) Mitt. with which it has been confused 
by Mitten also has its type locality in Jamaica but that species 
grows on rocks, in shade, is a smaller plant, with nearly simple 
branches, obtuse or shortly apiculate leaves which are shortly 
bicostate and without porose cells. Its distribution is from 
Jamaica, Porto Rico to Guadeloupe, and from Mexico and 
Guatemala to Costa Rica. 

27. Callicostella pallida (Hornsch.) Jaeg. 

Guatemala: Alta Verapaz, 388, Cook and Griggs, 1902. 
28. Callicostella Oerstediana C. Miill. 

Guatemala: Rio Pollochico below Panzos, 3086, Maxon and 

Hay, 1904. 
29. Harpophyllum aureum (Lam.) Spruce. 
Costa Rica: La Palma, 400, Maxon, 1906. 
30. Hypopterygium Tamarisci (Sw.) Brid. 

Costa Rica: Santiago, 116, Coliblanco, 338, Maxon, 1906. 
31. Helicophyllum torquatum Brid. 

Guatemala: 3538, Maxon and Hay, 1905. 

32. Rhacopilum tomentosum (Sw.) Brid. 
Rhacopilum latistipulatum Cardot 
Rhacopilum angustatum Sch.; Besch. 
Rhacopilum tomentosum longe-aristatum C. Miill. 

Nicaragua: Volcan Mombacho, 2367, Baker, 1903. 


30 


Guatemala: Alta Verapaz, Cook, 1905; San Felipe, 2536, 
Maxon and Hay, 1905. 
Costa Rica: Santiago, 89, Maxon, 1906. 
33. Thuidium miradoricum Jaeg. 
Costa Rica: Cartago, 499a, Maxon, 1906. 
34. Miitenothamnium Langsdorfi (Hook.) Cardot 
Costa Rica: La Palma, 384, Maxon, 1906. 
35. Mittenothamnium megapalmaium (C. Mill.) Card. 
Guatemala: Alta Verapaz, 325, Maxon and Hay, 1905. 
36. Mittenothamnium nicaraguense (Broth. ined.) E. G. B. comb. 
nov. 
Nicaragua: Volcan Mombacho, 2501, 2514, Baker, 1903. 
37. Mitienothamnium reptans (Sw.) Card. 
Costa Rica: Coliblanco, 339, 348, La Palma, 372, 374, Maxon, 
1906. 
38. Mittenothamnium Salleanum (Besch.) Card. 
Guatemala: Godman and Salvin in Hb. Mitt. 
39. Mittenothamnium substriatum (Mitt.) Card. 
Mexico: (Found without collector or locality in Hb. Mitt.) 
Det. by Max Fleischer. 
40. Ectropothecium apiculatum (Hornsch.) Mitt. 
Guatemala: Alta Verapaz, 93, 258, 383, Cook and Griggs, 1902. 
Costa Rica: Finca Navarro, 619, Maxon, 1906. 
41. Ectropothecium globitheca (C. Miill.) Mitt. 
Nicaragua: Volcan Mombacho, 2368, 2520, C. F. Baker, 1903. 
42. Ectropothecium pseudo-rutilans (C. Miill.) Paris 
Nicaragua: Volcan Mombacho, 2366, C. F. Baker, 1903. 
43. Isopterygium miradoricum (C. Miill.) Jaeg. (ex descriptio) 
Guatemala: Puerto Barrios, 3072, 3076, 3078, Maxon and 
Hay, 1904. 
44. Isopterygium pusillum Ren. & Card. 
Honduras: Puerto Sierra, 506, P. Wilson, 1903. 
Costa Rica: La Palma, 371, Maxon, 1906. 
45. Isopterygium trichopelma (C. Miill.) Paris 
Costa Rica: Coliblanco, 250, Maxon, 1906. 
46. Taxithelium planum (Brid.) Mitt. 
Honduras: Puerto Sierra, 507, 556, P. Wilson, 1903. 
Guatemala: Alta Verapaz, 3216, Maxon and Hay, 1905. 


dL 


47. Vesicularia amphibola (Spr.) Broth. 

Guatemala: Alta Verapaz, 410, Cook and Griggs, 1902. 
48. Vesicularia vesicularis (Schwegr.) Broth. 

Guatemala: Mazatenango, 3494, Maxon and Hay, 1905. 
49. Pterigonidium pulchellum (Hook.) Broth. 

Honduras: Puerto Sierra, 499, P. Wilson, 1903. 

Guatemala: Puerto Barrios, 3066, Maxon and Hay, 1904. 
50. Sematophyllum caespitosum (Sw.) Mitt. 

Costa Rica: Santa Clara, 604, 611, Cook and Doyle, 1903. 
51. Sematophyllum galipense (C. Miill.) Mitt. 

Honduras: near Puerto Sierra, 290, P. Wilson, 1903. 
52. Sematophyllum Lindigu (Hpe.) Mitt. 

Costa Rica: Coliblanco, 244, 265, 336, 346, Maxon, 1906. 
53. Lrichosteleum fluviale (Mitt.) Jaeg. 

Guatemala: Puerto Barrios, 3077, Maxon and Hay, 1904. 
54. Trichosteleum microcarpum Brotherus. 

Sematophyllum microcarpum Mitt. Jour. Linn. Soc. 12: 493. 
1869, in part. 

Nicaragua: Volcan Mombacho, 2497, C. F. Baker, 1903. 

In Mitten’s herbarium we find a specimen labeled Leskea micro- 
carpa “fl. Ind. occ. Swartz. Hb. Hooker.’’ This must have been 
a manuscript name of Swartz, because it does not occur in his 
flora Indiae occidentalis, as stated. It is evidently the type of 
Sematophyllum microcarpum Mitt. which he placed in the section 
Trichosteleum (p. 492), but it does not agree with other species 
of this genus, because although there are occasional small obscure 
papillae on a few of the young leaves, most of the leaves are 
entirely smooth and the specimen agrees with Sematophyllum 
xylophilum Mitt. (1. c. p. 490) to which it must be referred as 
a synonym. 


SHORTER NOTES 


WINTER CHANGES IN WEEPING WILLOW.—Since reporting the 
upward winter movement of the slender branches of the weeping 
willow tree* in front of the Columbia University Library, I have 
looked in vain for another tree showing the same curious phe- 

* The Weeping Willow in Winter, Torreya 10: 38, 1910. 


32 


nomenon. As described then, in December, the drooping twigs 
(on all but one of the main branches) curl up until each twig 
reaches a position above its point of origin, and the tree has a 
round-topped, bristly appearance. The writer will be much 
indebted to any one contributing observations, photographs, etc., 
of a willow tree showing similar changes; dates of the observed 


changes are also desirable. 
JEAN BROADHURST 


A NEw Form oF PyroLa BRACTEATA.—P. bracteata Hook. var. 
Hillii. var. nov. Stem and flowers as in the species; leaves 
wanting. Dry woods, Mayne Island, British Columbia. 

Mr. Albert J. Hill, M.A., who collected the plant several years 
"ago, says it is not rare in the above locality. It is quite distinct 
from P. aphylla Smith by its long bracts; and from P. aphylla 
var. paucifolia Howell by its calyx lobes, which are half as long 


as the petals. 
J. K. HENRY 


VANCOUVER 


CURRENT LITERATURE AND NOTES 


Howarp, C. Les Zoocécidies des Plantes d’ Europe et du 
Bassin de la Médtterranée. Tome III, Supplement 1909-1912; 
pp. 1249-1560. 1567 figures, 3 plates and 8 portraits. Librairie 
Scientifique, A. Herrmann et Fils: Paris. 10 Fr. This most 
excellent work, the third and supplementary volume of which 
has just appeared, is a model for a similar work on our American 
cecidia. This third volume contains brief, clear descriptions of 
1,317 species of galls distributed among 149 genera of gall 
makers and in 92 families of host plants. The species are grouped 
with reference to the taxonomic order of the host plants on which 
they occur but zoological and botanical indices makes the work 
very valuable for both entomologist and botanist. A very 
unique system of abbreviation on the margins of the pages 
indicate the location of the gall on the host plant and its geo- 
graphical distribution. The illustrations are mostly line draw- 
ings but are of such character as to greatly facilitate the deter- 


Do 


minations of the species. One of the most interesting parts of 
the work is the treatment of 16 galls on cryptogams. The work 
closes with a bibliography of 204 titles. 

This line of work which has received so much attention in 
Europe has been greatly neglected in America, but with the 
increasing interest in evolution, biochemistry, physiology and 
plant pathology the time is not far distant when it must become 
one of our most interesting and productive lines of botanical 
research. It is a field in which our American botanists must 
soon follow the lead of their European colleagues. However, 
it is unfortunate that in both Europe and America, the myco- 
cecidia have received much less attention than the zoé-cecidia. 

MeL T. Cook 


Hawkins, L. A. The influence of calcium, magnesium and 
potassium nitrates upon the toxicity of certain heavy metals toward 
fungus spores. Physiological Researches 2: 57-92, 1913. Mr. 
Hawkins has shown that, in certain cases, the effect of a toxic 
salt on the germination of the conidia of Glomerella cingulata 
may be influenced by the addition to the medium of calcium, 
magnesium or potassium nitrate. For the combination of Cu- 
(NOsz)2 with Ca(NOs)2 and of Zn(NOs)2 with Ca(NOs). and 
Meg(NOs)2, he has shown that this effect is not due to the forma- 
tion of undissociated double salts. He has also shown that it is 
not due to the depression of the ionization of the toxic salt. The 
salts which he tested, given in the order of their toxicity, are as 
follows: Cu(NOs)s, CuSOsu, Pb(NOs)e, Al(NOs)3, HNOs, Zn(NOQOs)o, 
Ni(NOs)o, Mg(NOs)s, Ca(NOs)o, and KNOs. 

L. O. KUNKEL 


Hans Kniep, Beitrage zur Kenntnis der Hymenomyceten I, II. 
Zeitschrift fiir Botanik, 5: 594-637. Au 1913, reports another 
effort to discover the origin of the binucleated cells in the hy- 
menomycetes. The work, as the title indicates, is divided into 

two parts. The first is devoted to a study of a new species, 
' Hypochnus terrestris Kniep. The author traces the development 
of this form from spore to spore and shows that there are no 
sexual organs or their equivalents. The spore prior to germina- 


34 


tion becomes binucleated. The germ tube and subsequent cells 
are all binucleated. The nuclei divide conjugately. He holds 
that these forms of fungi are reduced types rather than primitive 
ones. 

The second part is devoted to a cytological study of the life 
cycle of Coprinus nychtemerus Fr. He studied the germination 
of spores of this species and found that the cells of the germ 
tube are uninucleated, binucleated and more rarely multi- 
nucleated. He also reports the presence of clamp connections 
in which he discovered peculiar structures resembling nuclei. As 
to what the significance of these bodies is Kniep is not clear. 
He argues that the clamp connections serve no other purpose 
than to facilitate the transportation of food stuffs. Mycelial 
cells in later stages are uninucleated and binucleated. He holds 
however that the binucleated condition does not become fixed 
until the formation of the carpophore. The nuclear phenomena 
in the basidium are similar to those reported by other observers. 
He finds eight chromosones in the first division. Kniep was 
unable to find secondary nuclei in the basidium. 

MiIcHAEL LEVINE 


Mottiscu, H., Ueber den Einfluss des Tabakrauches auf der 
Pflanze. Sitzb. Wien Akad. Mat. Nat. Kl. 120 Abt. 1: 3-30, 
813-838, + 2 pls. 1911, takes up the question of the effect of 
tobacco smoke on plants grown under greenhouse conditions. 
Seedlings of Vicia sativa, Pisum, Cucurbita Pepo, etc., were grown 
in water cultures, covered by a bell jar of 4 L. capacity and 1-3 
puffs of cigar or cigarette smoke passed under the jars. Excellent 
photographs illustrate the striking results. Growth in length 
is practically stopped in the plants subjected to smoke; they 
commonly show a greater stem-diameter, however, than the 
controls. If the seedlings are grown in porous flower pots the 
results are similar for about the first three days, then the smoked 
plants begin to grow rapidly—a result attributed to the absorp- 
tion of the injurious substances by the soil and pot. 

Similar effects were obtained with the smoke of paper, wood, 
straw. Using singly various of the constituents present in 
tobacco smoke, it was found that nicotine is quite without effect, 


35 


carbon monoxide leads to results similar to those obtained with 
tobacco smoke, etc. Molisch considers the data inadequate, 
however, for determining what constitutes the effective ingredient 
or ingredients of tobacco smoke. 

Older plants generally are much less affected by tobacco 
smoke than seedlings. A number of specific peculiarities are 
encountered, however. In Goldfussia glomerata lenticel forma- 
tion is induced; Syringia vulgaris, Rosa, etc., shed their leaves 
(spring time) after about two days’ exposure to tobacco smoke. 


W. G. M, 


Plant Breeding in Scandinavia. By L. H. NEwWMANN. Pub- 
lished by the Canadian Seed Grower’s Association, Canada 
Building, Ottawa, Canada. Price $1.00 net (cloth $1.50). The 
plant breeding station of The Swedish Seed Association at Svaléf 
is now generally recognized as one of the foremost stations in the 
world for the practical and scientific breeding of the cereals. 

Mr. Newmann has recently spent about nine months at 
sval6f where he studied the methods of work and examined the 
various printed and private records of the investigations. This 
personal experience enables him to perform a distinct service in 
presenting the work of the station in book form to English reading 
students. 

The main divisions of the volume are as follows: I, Introduc- 
tion; II, The Swedish Seed Association (general résumé); III, 
The System of plant improvement at Svaléf and its development; 
IV, The composition of a race of cereals and its variability; V, 
Practical application of principles now recognized in cereal 
breeding at Svaléf; VI, Methods of work in cereal breeding at 
Svaléf; VII, Summary of work done with different crops and 
results obtained (wheat, barley, pease, clovers, grasses, and 
potatoes); VIII, Appendix; IX, Literature cited. 

A brief synopsis of the points that are of special interest can 
be grouped under the following heads: 


Methods and Results 
The method of ‘‘mass selection” is still used in maintaining 
purity of sorts, and as preliminary to ‘‘line culture’’ and hybridi- 
zation. 


36, 

Pedigree culture or line breeding on a large scale is a main 
method. In pure lines there are no hereditary variations, and 
“no correlations between botanical characters and industrial 
qualities.’’ Value of pure lines determined only by the yielding 
tests. This sort of line breeding isolates superior biotypes. 

Artificial hybridization—An important method in scientific 
breeding. Importance at Svaléf considered as based on the Men- 
delian conception of alternative inheritance and the recombina- 
tion of unit characters. It is followed by careful line breeding 
of hybrid progeny. 


Vanability 


No progressive mutations in cereals have appeared at the 
Sval6f station. 

Variations in cereals are largely due to natural nahi ricliee ee 
Aberrant forms in grains are often cases of segregation in the 
progeny of heterozygotes. 

Acclimatization is due to regrouping of factors in a heer 
zygous population. The stronger combinations survive. 

Hereditary variations may be continuous where different 
combinations of different units are such that gradations in a 
given character result. Continuous hereditary variations are 
possible but are considered as based on the chance combination 
of independent units (or fractions of a unit) which ultimately 
form a multiple factor. 

In regard to the practical and theoretical study of variations, 
the work with potatoes at Svaléf is proving of special significance 
as the potato is propagated vegetatively in what is essentially a 
pure line. In the five years that potato breeding has been in 
progress “continuous selection of desirable hills and tubers” 
has resulted in improvement. 

In criticism it may be noted that this sort of continuous 
hereditary variation is not to be explained on the basis mentioned 
above and suggests that a Mendelian conception of continuous 
hereditary variations is of doubtful validity. Infact much of the 
data presented concerning variation not only in the vegetative 
reproduction of potatoes but in the sexually reproduced cereals 


37 


suggests that the interpretation in terms of unit factors may be 


a rather gross analysis. 
TNA BSS 


Two works have just appeared of interest to taxonomiscs and 
some other botanists. The last supplement of Index Kewensis 
brings this indispensable work down to the end of 1910, and in- 
cludes citations to thousands of species and near species described 
during the four years that have elapsed since the previous 
supplement. There are more than two thousand species of 
- Hieracium cited, and as to Crataegus and other prolific genera 
an equally astonishing number of new names are listed. A new 
departure is the failure to italicize what the authors of the work 
consider untenable names, in the present volume, although they 
have indicated their preferences in this regard. 

A supplement has also been issued by Dr. Carl Christensen, 


of the Index Filicum. 
NE 


NEWS ITEMS 


We quote in part, from the following letter of Dr. E. D. Merrill 
in regard to the death of Dr. C. B. Robinson, noted in TORREYA 
for January: ‘‘Dr. Robinson was murdered on December 5, 1913, 
about 8 miles from the town of Amboina by six Mohammedan 
natives of the island of Boeton. The island of Amboina is 
entirely pacific, and there has been absolutely nothing to fear 
from the inhabitants of that island. Dr. Robinson’s voluminous 
progress reports make no mention whatever of any difficulties 
with the natives, and the idea that harm might result has never 
been entertained by ourselves in Manila, by Dr. Robinson him- 
self, or by the Dutch officials in Amboina. The coincidence of 
these six Mohammedans coming from the distant island of 
Boeton, their meeting with Dr. Robinson on one of his botanical 
excursions, and his resulting murder were matters that could 
not be foreseen and could not be guarded against. . . . The results 


38 


of his work in Amboina will not be lost, for his collections, notes, 
etc., are intact, and are being forwarded to Buitenzorg, whither 
I shall probably go to receive and care for them. However, no- 
body but Dr. Robinson can do justice to the work of correlating 
the collections with the plants described and figured by Rumph, 
although his progress reports, very extensive and detailed, prob- 
ably over 60,000 words, will help to clear up many points.”’ An 
account of Dr. Robinson’s life and work will appear in an early 
number of the Bulletin. 


The following new appointments of members of the gardening 
staff at Kew are quoted in Nature from Kew Bulletin: Mr. G. 
S. Crouch, to be assistant director of horticulture in the Egyptian 
department of agriculture; Mr. T. H. Parsons, to be curator of 
the Royal Botanic Gardens, Peradeniya, Ceylon, in succession 
to Mr. H. F. Macmillan, who has been appointed superintendent 
of horticulture in the department of agriculture, Ceylon; Mr. 
C. F. Allen, to be curator of the Botanic Garden, Port Darwin, 
Northern Territory, South Australia, in succession to Mr. N. 
Holtze, deceased. 


At the meeting of the American Phytopathological Society 
recently held at Atlanta the following officers were elected: 
President, Dr. Haven Metcalf, Washington, D. C.; Vice-president, 
Dr. Frank D. Kern, State College, Pa.; Counsellor, Professor 
H. R. Fulton, West Raleigh, N. C. 


Dr. J. C. Arthur and Mr. F. D. Fromme of Purdue University 
are spending the month of February ona botanical trip to the 
southwest. They will visic a number of localities in Texas, New 
Mexico and Arizona where certain species of Uredinales, whose 
life histories are incompletely known have been previously col- 
lected. 


Mr. E. H. Wilson, whose recent book on western China was 
reviewed in ToRREYA for January, has gone to Japan for a two 
years’ collecting trip. 


ue 
ie hies 


ie yanuies 


hehe aL pal 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six 
gratuitous copies of the number of Torreya in which their papers 
appear, will kindly notify the editor when returning proof. 

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The following Committees were appointed in 1913 


Finance Committee t Field Committee 
J. I. Kane, Chairman SERENO STETSON, Chatrman 
Ropert A. HARPER 


Budget Committee Program Committee 
J. H. Barnwart, Chairiman Mrs. E. G. Britton, Chairman 
N. L. Britton Miss JEAN BROADHURST 
B. O. DopGE  _ C. SruaRT GAGER 
M. A. Howe. * F. J. SEAVER 
E. L. Morris 
H.-H. Russy 


Local Flora Committee 
N. L. Britton, Chawiman 


-Phanerogams: - - Cryptogams: 
E. P. BICKNELL Mrs. E. G. BRITTON 
N. L. Britton Puitip DOWELL 
C. C. Curtis Tracy E. Hazen. 
K. K. MAcKENZIE M. A. Howe 

-_E, L. Morris W. A. MurriLy 


“NorRMAN TAYLOR 


Delegate to the Council of the New York Academy of Sciences 
WILLIAM Nees 


OTHER PUBLICATIONS 
OF THE ? 


TORREY BOTANICAL CLUB. 


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- March, Igl4 No. 3 


‘ORREYA | 


a Monrary Journar OF Por aascar Notes and News 


EDITED FOR _ 
THE TORREY BOTANICAL CLUB 
me 8 : BY | 
NORMAN TAYLOR 
JOHN TORREY, 1796-1873 
CONTENTS 
Saute fossil leaves and their significance: FE. W. HUMPHREYS..........:0sceseesee sere eee 30 
1913 Notes on the flora of Copake Falls, N.Y. : SERENO STETSON.«.-.0+.2+-;-+5 Bee 42 
wo British Columbia Notes < J: K. HENRY..e-0cyidessstscesccesesgeeccbocecpeeesereeeeen! AS 
Reviews : : ; 
“Steven’s Fungi which cause disease: E,W. OLIVE. ..:.c0.cscstcepeseereee ety eceees 46 
_ > Harper’s Report on Alabama Forests: S. J. RECORD ..:6c0-:0:e1essteseeeee sere a7 
- Proceedings of the: Club. 52s as A Olas ah igh ee eR Pe ee eee. 49 
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Columbia University, New York City 


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tviy 


aver keh a 


TORREYA 


March, Ig1!4. 
Vol. 14 No. 3 


SOME FOSSIL LEAVES AND THEIR SIGNIFICANCE 


By EpWIN W. HUMPHREYS 


Anything that will shed light, however feeble, upon the life 


processes of the past in their relation to those of the present is 


always of interest; hence, when certain abnormal fossil leaves 


-are found which show the same aberrations that living ones of, 


apparently, the same genus possess, that fact seems to be worthy 
of record. 

In the American Naturalist for 1907,* there are three articles 
on the development of pinnate leaves as shown by examples of 
arrested development in mature leaves of living plants. The 
occurrence of similar forms among fossil leaves and their sig- 
nificance is the subject of this paper. 

In Lesquereux’s Flora of the Dakota Groupt two specimens 
of fossil Rhus leaves (Rhus Powelliana Lesq.) are figured, in one 
of which, reproduced on plate A, fig. I, a, the terminal leaflet 
has reached a stage of development similar to that shown by 
the terminal leaflet of the living Rhus glabra L. (pl. A, fig. 1, 0). 
The other (pl. A, fig. 2, a) shows a stage like that of the sumac 
leaf depicted in pl. A, fig. 2, b. There is, however, a more ad- 
vanced stage of development portrayed in the leaf represented 
in pl. A, fig. 1, a, for some of the lateral leaflets are lobed; one of 
them, in fact, showing a distinct leaflet. In this case, the primary 
leaflets seem to exhibit a tendency to become pinnate, thereby 
foreshadowing the formation of a bipinnate leaf. Fig. 1, c isa 
drawing of a portion of a leaf of Rhus glabra L. showing a similar 
stage of development. 

There is another species of fossil Rhus, R. Uddeni Lesq. (pl. A, 

*F, T. Lewis, Am. Nat. 41: 431, 701, 817. 1907. 


7 Mon. U. S. Geol. Survey 17: 155. pl. 506, figs. 4-5. 1892. 
[No. 2, Vol. 14, of TorREYA, comprising pp. 21-38, was issued 9 February, 1914] 


39 


40 


fig. 3), from the Dakota Group* which shows a lobed terminal 
leaflet. This species has a petiole that is partly winged, suggest- 
ing Rhus copallina L. 

Thus, there would seem to be two species of fossil Rhus leaves 
whose method of development was similar to that of the living 
Rhus glabra L. and Rhus copallina L. and, therefore, basifugal. 

Another species which presents an interesting example of 
arrested leaf development is Negundo triloba Newb.} (pl. A, fig. 
4, a) from the Fort Union Group. This leaf has a lobed terminal 
leaflet that is almost wholly split off, suggesting a basifugal 
tendency such as can be found in the living Acer Negundo (pl. A, 
fig. 4, 5). 

In the same work (pl. 30, fig. 2) a specimen of the fossil species 
Sapindus membranaceus Newb., is figured, which shows a lateral 
leaflet completely split from the terminal one (pl. B, fig.1,a@). An 
investigation of the specimens of Sapindus in the herbarium of the 
New York Botanical Garden revealed some leaves of Sapindus 
saponaria L. in which the terminal leaflet had split to form a new 
lateral (pl. B, fig. 1, 6). Here again is a case of a living form 
and a fossil form of apparently the same genus developing their 
leaves in the same way. 

In Fontaine’s Potomac or Younger Mesozoic Florat several 
leaves are figured whose affinity to Sapindus is indicated by the 
generic name Sapindopsis. Certain leaves of this genus, belong- 
ing to two different species (S. variabilis Font. and S. magnifolia 
Font.) exhibit lobed terminals in various stages of development 
(see pl. B, figs. 2,a and 2,06). In fact, a short though incomplete 
series of the figured leaves of Sapindopsis variabilis Font. might 
be arranged to show the successive steps in the formation of the 
lateral leaflets from the terminal leaflet. 

A further search of paleobotanical literature and of duplicate 
specimens of fossil plants would doubtless disclose many other 
interesting examples. 

* Mon. U.S. Geol. Survey 17: 154. pl. 57, fig. 2. 1892. 

+ Newberry, Mon. U. S. Geol. Survey 35: 115. pl. 31, fig. 5. 18098. 

t Mon. U. S. Geol. Survey, 15: 297, pl. 151, figs. 2, 3; pl. 152, figs. 2, 3; 


pl. 153, fig. 2; pl. 154, figs. I, 5; pl. 155, fig. 6: 208, pl. 151, fig. 1; pl. 152, 
figs. 1-4; pl. 153, fig. 3; pl. 154, figs. 2-4; pl. 155, figs. 2-5. 1889. 


41 


It had been hoped that similarity in development might serve 
as an aid in the identification of fossil leaves of the forms dis- 
cussed. That is to say, if the fossil pinnate leaf did not develop 
in a manner similar to its nearest living relative, it would furnish 
a warning to review the identification. Goebel,* however, states 
that “. . . the course of development in nearly allied plants 
varies, for example, in pinnate leaves it is sometimes acropetal 
and sometimes basipetal.’’ It is, however, suggestive that in 
two of the cases here noted, Negundo and Sapindus, the lobing of 
‘the terminal leaflet was first noticed in the fossil species and that 
this resulted in a successful search for similar examples among 
the related living forms. 

The unsymmetrical outline of certain terminal leaflets from 
which a lobe has split, such as is well shown in the terminal 
leaflet on pl. B, fig. 1, a, does, however, offer a suggestion to 
those engaged in identifying fossil leaves. Should such a fossil 
leaflet, minus its lobe, be preserved alone, the tendency would 
likely be to regard it as a simple leaf, rather than as a leaflet 
of a compound leaf. Hence, in endeavoring to determine the 
probable relationship of any such unsymmetrical leaf, it might 
be advisable to consider whether or not it could be a leaflet of a 
compound leaf. 

Briefly then the leaves under discussion show: (1) that like 
forms of leaves, of arrested development, occur in certain species 
of living and fossil plants of the same genus; (2) that these forms 
indicate that similar methods of leaf development took place in 
each of them; (3) that if ‘‘nearly allied”? plants may develop 
their leaves in different ways, it follows that the mode of develop- 
ment is of questionable value to paleobotanists in identifying 
forms of arrested development among fossil pinnate leaves; (4) 
that in identifying simple fossil leaves of the form of the terminal 
shown on pl. B, fig. 1, a, if the lobe were not preserved, it might 
be advisable to view it as a possible leaflet of a pinnate leaf. 


* Organography of Plants, authorized English edition, pt. 2, p. 330. 1905. 


EXPLANATION OF PLATES 


Plate A 


Fig. ta. Rhus Powelliana Lesq. showing lobed terminal leaflet, and on the 
right a lobed lateral. On the left is a lateral from which has split a secondary 
leaflet. 


Fig. 1b. Rhus glabra L. showing lobed terminal leaflet similar to that shown 
in fig. za. 

Fig. tc. Two lateral leaflets of Rhus glabra L. On the left a secondary 
lateral is shown, on the right a lobed lateral. 

Fig. 2a. Rhus Powelliana Lesq. showing lobed terminal. 

Fig. 2b. Rhus glabra L. showing terminal leaflet like that in fig. 2a. 

Fig. 3. Rhus Uddeni Lesq. showing lobed terminal leaflet. 

Fig. 4a. Negundo triloba Newb. showing a terminal leaflet lobed on the left 
side. 

Fig. 4c. Acer Negundo L. showing lobe similar to that in fig. ga. 


Plate B 


Fig. ta. Sapindus membranaceus Newb. showing lateral leaflet split from 
terminal leaflet. 


Fig. 1b. Sapindus saponaria.L. showing terminal leaflet from which a lateral 
leaflet has split. 

Fig. 2a. Sapindopsis variabilis Font. showing lobed terminal leaflet. 

Fig. 2b. Sapindopsis magnifolia Font. showing lateral leaflet split from 
terminal. 


1913, NOTES ON THE FLORA OF COPAKE FALLS) Nese 


By SERENO STETSON 


The growing season at Copake during the past year came fully 
up to expectations. On account of the comparatively little 
snow that fell during the winter months (1912-13) some concern 
was felt for the spring flora, but a visit on April 22 allayed all 
fears in that direction. There was a profusion of young growth 
and Tussilago Farfara L., Trillium erectum L., Sanguinaria 
canadensis L. with numerous representatives of Vzola were 
flowering in large numbers, and there was no sign of the herb- 
age in general having suffered from the failure of the snow 
blanket. 

The next visit covered May 17 and 18 and furnished several 
surprises. While working the western slopes of Cedar mountain 


Plate A. See explanation, page 42. 


Plate B. See explanation, page 42. 


43 


at an altitude of 1,300 feet a large colony of Cypripedium parvi- 
florum var. pubescens (Willd.) Knight was discovered. A rough 
estimate would place their number at sixty and in the course 
of scouting the area the surrounding deciduous woods were 
found to contain numerous scattered plants of Cypripedium 
acaule Ait. These stations are’ entirely new and are not the 
ones referred to in Torreya 13: 126. The inaccessibility of 
the location nodoubt accounts for their uninterrupted propa- 
gation. 

Descending by way of the ravine through which runs Cedar 
‘brook a search was made for a colony of Trientalis americana 
(Pers.) Pursh which had been noted some years before. It was 
found growing in profusion, stretching up and down the brook 
on either side for a considerable distance. Polygala paucifolia 
Willd. was also present in great numbers, and was somewhat of 
a surprise as it has never been known on this side of Bash-Bish 
brook. 

Dr. B. O. Dodge, of Columbia University, who was present on 
this occasion, reports having collected numerous interesting 
specimens of fungi. 

The following day was spent in the swamps to the west of 
the railroad. ' Iris versicolor L. was in full bloom and _ fairly 
covered the semi-dry portions, and the remains of Menyanthes 
trifoliata L., long gone to seed, were visible everywhere. Large, 
beautiful specimens of Lupinus perennis L. grew along the rail- 
road and a dry ridge, near by, was literally yellow with dwarfed 
specimens of Krigia virginica (L.) Willd., the tallest measuring 
only 3 cm. in height. 

The final visit for the year commenced on August I9 and 
continued until September 7. This is undoubtedly the most 
interesting season of the year at this place and furnishes the 
greatest number of plants to the botanical student. 

The accompanying photograph of Gentiana quinquefolia L., 
was taken September 5 while exploring the wooded slopes of 
Cedar mountain and attracted the writer’s attention on account 
of its unusual leaf arrangement. It will be noticed that they 
are borne in whorls of three throughout the plant. There is no 


44 


mention in any of our manuals of any species of Gentianacez 
growing in this climate whose leaves are anything but opposite 
and a thorough search of the herbaria of both the New York 
Botanical Garden and the Brooklyn Botanic Garden failed to 


Fic. 1. Unusual leaf arrangement in Gentiana quinquefolia L. Copake Falls, N. Y. 


reveal another specimen of similar phyllotaxy. The writer would 
be glad to hear from anyone knowing of another case. 

A trip made on the western slopes of Bash-Bish mountain 
September 3 brought to light four plants which had not been 
noted in this region before. Soon after the start the red berry- 


45 


like annular disk of the American yew, Taxus canadensis Marsh, 
was noted. These increased in number at the higher altitudes, 
occurring in depressions or very damp shaded spots. Ina large 
stand of deciduous trees a number of specimens of Habenaria 
hyperborea (L.) R. Br. were collected. One of these is an espe- 
cially beautiful specimen, very tall and straight, with about 
thirty-five blossoms on it. A surprise was furnished in finding 
Hypericum punctatum Lam. in a damp, shady situation. H. 
perforatum L. is very common throughout this region but of the 
many times in years gone by that a search had been made for H. 
punctatum it has never been located in this vicinity until now. 
In the descent a number of specimens of Aster acuminatus Michx. 
were picked up, growing among some dense, wet underbrush 
alongside a “‘trickle.’”’ These are apparently confined to this 
mountain as a search of the woods north of Bash-Bish brook 
failed to disclose another specimen. 

In closing it would be well to correct an error in Mr. S. H. 
Burnham’s Supplementary List of the Plants of Copake Falls, 
N. Y., published in ToRREYA for September, 1913. The legend 
attached to my photograph in Torreya 13: 127 is correct. 
Lookout Rock is in Massachusetts and next the state line. The 
view is directly west toward the Hudson River and shows the 
“Gap” referred to for its entire distance in New York State. 
Sunset Rock is a very different spot situate on a high promontory 
directly overlooking the valley shown in the distance and about 
two miles due northwest of Lookout Rock. 


NEw YORK 


TWO BRITISH COLUMBIA NOTES 
By J. K. HENRY 


RHODODENDRON ALBIFLORUM Hook. 


The flowers of this beautiful shrub are always described as 
white. My specimens from the Selkirks and the Coast Range, 
B. C., and Mt. Ranier, Wash., are white. One day last summer, 
however, on a mountain side at Roger’s Pass in the Selkirks, I 
found one plant on which the three anterior petals had a few 
yellow dots towards the base of the segments. On the mountains 


46 


opposite Vancouver City this form is common, but the spots are 
orange. I therefore propose— 


R. albiflorum Hook. forma poikilon f. n. 


The three anterior petals spotted towards the base with yellow 
or orange. 


SOME COROLLA FORMS OF CAMPANULA ROTUNDIFOLIA L. 

At Field in the Rockies, and at Revelstoke in the Selkirks 
many forms of this species occur. The variations in the corolla 
at once attract even the casual observer. Forms with funnel- 
shaped corollas (C. dubia A. DC.) grow side by side with the 
forms characterized by the round base. Ordinarily there is no 
difficulty in distinguishing the plants. A striking white-flowered 
form of C. dubia was observed at Revelstoke. Miss Farr, in her 
catalogue for this region, based in part on Macoun’s Catalog of 
Canadian Plants, mentions only C. petiolata and C. rotundifolia. 
There is also a form at Field with campanulate corollas broader 
than long—20-23 mm. broad, 14-16 mm. long; but I have seen 
too few plants to form an opinion as to the validity of the form. 
The funnel-form corollas are also sometimes as broad as long, 
or even broader. 


VANCOUVER 


REVIEWS 


Steven’s Fungi which Cause Plant Disease * 

As stated in the preface, this volume is intended to introduce 
to the student the more important cryptogamic parasites affecting 
economic plants in the United States, with sufficient keys and 
descriptions to enable the student to identify them. The book is 
in fact rather unique in respect to these keys, and is apparently 
intended to be supplemented by the author’s Diseases of Econ- 
omic Plants or by other available books on plant pathology, 
since in the volume before us but little cognizance is taken of 
the pathological effects on the host or remedial measures. 

The readily available keys should undoubtedly prove exceed- 
ingly useful to students of plant diseases. Of perhaps even 


*F.L. Stevens. The Fungi which Cause Plant Disease. Pp. vii-ix + I-754 
f. 1-449. The Macmillan Company. New York. 1913. Price, $4.00. 


47 


greater value to plant pathologists are the voluminous citations 
and bibliographies, together with the abundant illustrations, 
which include at least one for each genus of importance in the 
United States. 

With the present vigorous prosecution of the study of plant 
diseases, it is obviously inevitable that a book of this nature 
should be out of date in some subjects the moment it leaves the 
hand of the printer. But this hardly excuses the utter disregard 
in a few places of researches of a number of years’ standing, such 
as those on Monascus, and those on Puccinia graminis by Pritch- 
ard. It is, further, very unfortunate that poor proof-reading 
should mar the text in other places, such, for instance, as on p. 
80, where the past tense is used instead of the present; on p. 112, 
“Bot. Gaz.’ for bot. Ges.; on p. 142, ‘‘conidial’’ instead of 
conical; on p. 143, ‘““unknown on,” apparently for known only 
on; on p. 391, ‘Key to species,’ instead of Key to assignment 
of species. On p. 366 is shown a rare instance of poor selection 
of illustration. Each cell of the teleutospore should obviously 
have but one basidium. A few of the illustrations might be 
made more effective if labelled more clearly; such, for example, 
as figs. 77, 100, 173, 174, 249, 383 and 662. 

These defects fortunately detract but little from the great 
value and usefulness of the book, and there can be no doubt of its 


hearty welcome by plant pathologists. 
E. W. OLIVE 


Harper’s Report on Forests of Alabama * 

This is an exceptionally valuable report since it not only con- 
tains a vast amount of information about the forests of Alabama 
but has it classified and arranged according to geographical 
divisions of the state. This method has very decided advantages 
over general descriptions, though it requires an extensive and 
detailed knowledge of local conditions to be followed satis- 
factorily. 


* Harper, Roland M. Economic Botany of Alabama. Part I: Geographical 
Report, Including Descriptions of the Natural Divisions of the State, their Forests 
and Forest Industries, with Quantitative Analyses and Statistical Tables, Mono- 
graph 8, Geological Survey of Alabama, University, Alabama. June, 1913. Pp. 
228; map and 63 half-tones. 


48 


In this report fifteen main divisions are recognized and some 
of them are subdivided into two or three. The divisions fall 
naturally into two classes, namely, the hill country or mineral 
region covering about two fifths of the state, and the coastal 
plain region. The latter is poor in minerals, water power, and 
mountain scenery, but rich in agricultural and timber resources. 
The line between them is called the ‘‘fall line,’ because most of 
the rivers which cross it have falls there. 

The regions comprising the hill country are: (1) Tennessee 
valley; (2) coal region, northern and southern portions; (3) 
Coosa Valley; (4) Blue Ridge; (5) Piedmont. Those comprising 
the coastal plain group are: (6) central pine belt; (7) black 
belt; (8) Chunnennuggee Ridge; (9) post oak flatwoods; (10) 
southern red hills; (11) lime hills; (12) limesink region; (13) 
southwestern pine hills; (14) Mobile delta; (15) coast strip. 

In describing each geographical division the same general 
plan is followed, though the amount of space devoted to each 
varies with the character of the country. The main headings 
are: Location, area, and external relations; references to previous 
literature; geology and soils; topography and hydrography; 
climate; forest types; fire; list of trees (with relative abundance 
and habitat of each); economic aspects, such as density of 
population, relative area of forests and clearings, status of stock 
laws, changes in relative abundance of certain species, principal 
forest products and wood-using industries. The location and 
boundaries of the different divisions and subdivisions are shown 
on amap. The text is supplemented by sixty-three half-tone 
illustrations from original photographs. An excellent bibliog- 
raphy of Alabama geography is included. 

The author has decided views concerning the effect of fires 
on longleaf pine, and, as they are somewhat at variance with 
ideas held by foresters generally (based on experience with 
other types of forest), it may prove of interest to quote him. 
Among other things he says: 

“In general the effect of fire in a forest is to keep down under- 
brush and trees with thin bark or low branches, and thus favor 
the growth of trees with thick bark and clear trunks, such as 


49 


most of the pines. It also returns quickly to the soil the potash 
and other mineral substances accumulated in fallen leaves, but 
drives off the inorganic matter which would otherwise make the 
soil more nitrogenous. It may destroy some insects which would 
otherwise injure the trees. . . . (It) does very little harm to 
the longleaf pine after that reaches the age of four or five years. 

“Tt can be safely asserted that there is not and never has 
been a longleaf pine forest . . . which did not show evidences 
of fire, such as charred bark near the bases of the trees; and 
furthermore, that if it were possible to prevent forest fires 
absolutely the longleaf pine—our most useful tree—would soon 
become extinct. For where the herbage has not been burned 
most of the pine seeds lodge in the grass and fail to germinate, 
and if the oaks and other hardwoods were allowed to grow 
densely they would prevent the growth of the pine, which 
cannot stand much shade, especially when young. 

“At the present time most of the fires in the pine woods are 
set purposely, to burn off the dead grass and improve the grazing. 
This practice has been repeatedly denounced by persons who 
have spent most of their lives outside of longleaf pine regions, 
but really the only just criticism of it that can be made is that 
it is done too often.” 

There are two other parts of this report contemplated: “ Part 
II, a catalogue of the trees and shrubs, with their distribution 
and economic properties; Part III, the medicinal plants, the 
weeds and useful or noxious plants not included in the preceding 
parts.” SAMUEL J. RECORD 


YALE FOREST SCHOOL 


PROCEEDINGS OF THE CLUB 


DECEMBER 9, I913 
The first regular meeting for the month of December was held 
on the ninth at the Museum of Natural History at 8:15 P.M. 
President Burgess presided. Sixteen persons were present. The 
minutes of November 26 were read and approved. 
The announced program for the evening was an illustrated 


50 


lecture by Dr. M. T. Cook on “Peach Yellows and Methods of 
their Control.’’ Professor Cook briefly traced the history of 
the disease from the earliest times to the present. He showed 
that whereas the problem was formerly considered a trivial matter 
it is now recognized as one of the most profound subjects which 
presents itself to the plant pathologist. The peach yellows and a 
closely related disease, little peach, are of considerable menace 
to the peach growing industry in the east. This is due to the 
fact that these diseases cannot be detected in their earlier stages 
and consequently nurserymen and growers are continually 
propagating by budding from infected stock. 

A most peculiar phenomenon is the appearance of the external 
morphological symptoms of peach yellows in trees that have been, 
injured, girdled, or neglected. The leaves become leathery, 
curl, and usually fold at the midrib. The blossoms appear 
earlier and likewise the fruit. The infected peach is generally 
speckled and insipid. The one character which enables the 
horticulturalist to make certain the presence of peach yellows 
is the witches-broom effect of the twigsin winter. This character 
is absent from trees suffering from injury or little peach disease. 

At present there is no cure for peach yellows or little peach, 
and the only remedial measures taken to prevent the spread of 
the diseases are quarantine, and the destruction of infected trees. 
Dr. Cook hopes that within a short time he will be able to give 
the nurserymen and growers simple tests for detecting the 
diseases in their earlier stages. 

Meeting adjourned. MICHAEL LEVINE, 

Secretary pro tem. 


NEWS ITEMS 


Dr. Britton, accompanied by Mrs. Britton, Mr. John F. Cowell, 
Director of the Buffalo Botanical Garden and Mr. Frank E. 
Lutz of the American Museum of Natural History, sailed for 
Porto Rico on February 7 to continue studies of the botany and 
zoology of that island in codperation with the New York Academy 
of Sciences. The party will make Mayagiiez a base of operations 


51 


for explorations in western Porto Rico, and the islands of the 
Mona Passage, planning to return to New York about March 16. 


An American Botanical Exchange Bureau has been started 
by Mr. G. L. Fisher, 901 Pease Avenue, Houston, Texas. It 
serves a very useful purpose as a medium of exchange for herba- 
rium specimens of American and foreign plants. Further informa- 
tion may be had from Mr. Fisher. 


Dr. C. A. Schenck, who founded the Biltmore Forest School 
in 1898 and has been in charge of it ever since, announces the 
discontinuance of the school and his appointment to a position 
in the government forest service in Germany. 


Yale University has just completed a new laboratory of 
botany and zodlogy. The building is an imposing structure of 
brown sandstone, erected at a cost of about five hundred thousand 
dollars, and has been named after the donor, Mrs. C. J. Osborn. 
It is constructed in the shape of an L, one wing being devoted 
to botany, the other to zodlogy. The botanical wing, three 
stories in height above the basement, contains eight large 
laboratories, a smaller laboratory for graduate students, a small 
lecture hall, numerous private rooms, rooms for mycological 
and photographic work, and a capacious herbarium and museum 
. room. In the angle between the two wings is a large auditorium 
with a seating capacity of three hundred. It is expected that 
in the near future a plant house with facilities for experimental 
work will be added. 


Dr. Lazarus Schéney, for some time a member of the Club, 
died at Coney Island on February 18. He was a Fellow of the 
New York Academy of Sciences and a member of numerous other 
scientific bodies. He was born at Budapest, October 18, 1838. 


Professor W. W. Bailey, for many years the head of the depart- 
ment of botany at Brown University, died at Providence, R. L., 
on February 20. The Evening Post writes, in part, as follows: 
“Professor Bailey was the son of Prof. Jacob Whitman and Maria 
Slaughter Bailey. He entered Brown University in 1860, and in 
1862 became a private in the Tenth Rhode Island Volunteers. 

-He returned to Brown and was graduated in 1864. He received 


52 


the degree of Ph.B. in 1873, that of A.M. in 1893 from that 
university. He studied botany at Columbia in 1872 and at 
Harvard Summer School in 1875, 1876, and 1879. In 1866 he 
was an assistant in chemistry at the Massachusetts Institute of 
Technology, and from 1867-68 he was the botanist of the United 
States geological survey of the fortieth parallel. During the 
latter year he became Deputy Secretary of the State of Rhode 
Island, and from 1869-71 he served as assistant librarian of the 
Providence Atheneum. He taught botany in private schools in 
Providence, and in 1877 he became an instructor at Brown. 
From 1881-1906 he served as professor of botany at tH€ same 
university, and since the latter date he has been professor 
emeritus. Professor Bailey was a member of the second board 
of visitors to the United States Military Academy in 1896, and 
in 1902 a delegate to the centennial of the United States Military 
Academy. He was a director of the Providence Atheneum, 
1900-3; a member of the International Society of Botanists, 
the New England Botanical Club, the Rhode Island Horti- 
cultural Society, the Boston and Newport Societies of Natural 
History, the Torrey Botanical Club, the New York Micro- 
scopical Society, Phi Beta Kappa, having been president of the 
Rhode Island Alpha, 1903-5, Sigma Xi, president of Brown 
chapter, 1903-4. He was also a member of the G. A. R., the 
Sons of the Revolution, the Society of American Wars, the 
Council of the Agassiz Association, and an honorary member of 
the Rhode Island Medical Society.”” Professor Bailey was born 
at West Point, N. Y., on February 22, 1843. He was the author 
of many books and articles. 


The ‘‘second circular” of the Fourth International Botanical 
Congress, to be held in London in 1915, has appeared. It is 
taken up by a discussion of the nomenclature questions to be 
brought up at the Congress. Among these are to fix the starting 
point for the nomenclature of Schizomycetes, Schizophyceae 
(excepting Nostocaceae), Flagellatae and Bacillariaceae; and the 
compilation of lists of ‘“‘genera conservanda’”’ for fungi, lichens, 
Bryophyta, and of a double list of such genera for paleobotanists. 
After bewailing the fact that nomenclature has occupied most 


5d 


of the attention of the congresses since the Paris meeting in 1900, 
the incorrigibly optimistic committee close their circular thus: 
“Tt is highly desirable from all points of view that this work 
should be completed in London in 1915, and should cease to 
occupy the International Botanical Congresses. We therefore 
urgently beg botanists in general, and cryptogamists and palaeo- 
botanists in particular, to examine carefully these points which 
still require consideration, and to formulate their propositions 
in such a manner that nothing may be left over for 1920.” 
Further information may be had from Dr. A. B. Rendle, British 
Museum, Cromwell Road, London, S. W. The Rapporteur 
Général is Dr. J. Briquet, Director of the Botanical Garden at 
Geneva. 


We learn from Science that The Mendelian Society of Vienna 
has celebrated the thirtieth anniversary of Mendel’s death by 
opening a new institute devoted to research in heredity. 


Dr. E. East, of the Bussey Institution, Harvard University, 
delivered a lecture at the Academy of Music, Brooklyn, on Sat- 


urday, February 28, on “The evolution of the modern ear of 
corn.”’ 


According to the Evening Post Miss Edna Dwinel Stoddard 
has been promoted from instructor to assistant professor of 
botany at Smith College. 


We learn from Science that Dr. Ludwig Diels, of Marburg, has 
been appointed associate professor of botany in the University of 
Berlin, and assistant director of the Botanical Garden and 
Museum. 


® 

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- The following Committees have been appointed for 1914 


- Finance Committee. Field Committee 
at's H. Barnaart, Chairman SERENO STETSON, Chairuzan - 
“Miss C. C. Haynes : 
Budget Committee Program Committee 
_ J. WH, Barnuart, Chairman Mrs. E. G. Brirton, Chairman 
N. L. Brirron Miss JEAN BROADHURST 
B. O. DoncE C. SruarT GAGER 
-M. A. Howe. ; F. J. SEAVER 
A. W. Evans 
H.-H. Russy 


Local Flora Committee 
N. L. Britton, Chairman 


Phanerogams: Cryptogams: 
E. P. BickNELL /.- Mrs. FE. G. Britton 
N. L. Brirron ~~ Puitre DOWELL 
C.-C. Curtis Tracy E, Hazen 

K. K. Mackenzie : M. A. Howe 
NorMAN TAYLOR © “ W. A. Murriby 


__ Delegate to the Council of the New York Academy of Sciences 
eS WILLIAM MANSFIELD 


OTHER PUBLICATIONS 


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ar ep I o> CONTENTS 
The International Phytogeographic Excursion in America: G. E. NICHOLS....-....++- 56 


List of Plants Collected on the Stekansoa Anderson Arctic Expedition, 1908-1912 
P. A. RYDBERG 65 


+ rah New Genus from Missouri : Kennets ROSA ACR RIAs Sn soetice spec p eee peaaeeee 67 
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TORREYA 


April, 1914. 
Vol. 14 No. 4 


THE INTERNATIONAL PHYTOGEOGRAPHIC 
EXCURSION IN AMERICA* 


By GEORGE E. NICHOLS 


During the summer of 1913 it was the privilege of the writer 
to participate in the International Phytogeographic Excursion 
in America. This excursion was organized and conducted by 
Professor H. C. Cowles, of Chicago, to whom too much credit 
cannot be given for his careful planning and efficient leadership. 
The personnel of the party included ten Europeans and seven 
Americans. The foreign members were Professor Adolf Engler, 
of Berlin; Professor C. von Tubeuf, of Munich; Professor C. 
Schroéter, Dr. E. Riibel, and Dr. and Mrs. H. Brockmann- 
Jerosch, of Zurich; Mr. and Mrs. A. G. Tansley, of Cambridge; 
Dr. O. Paulsen, of Copenhagen; and Professor T. J. Stomps, of 
Amsterdam. The American members, besides Professor Cowles 
and the writer, were Professor and Mrs. F. E. Clements, of 
Minneapolis; Professor and Mrs. A. Dachnowski, of Columbus; 
and Dr. G. D. Fuller, of Chicago. The excursion was joined 
by other American botanists in various parts of the country, and 
some of these accompanied the party for one or two weeks. 
Altogether the excursion was participated in by nearly two 
hundred. The expedition left New York, westward bound, on 
July 30, and the route traveled during the succeeding ten weeks 
is indicated on the map (fig. 1.) A short account of the trip is 
here given, together with some reference to the more salient 
features of the vegetation encountered.t Attention is confined 
chiefly to the botanical side of the excursion, but it need hardly 
be remarked that-the hospitable reception accorded the party 


* Contribution from the Osborn Botanical Laboratory. 
7 A more detailed account is being published by Tansley in the New Phytologist. 
[No. 3, Vol. 14, of ToRREYA, comprising pp, 30-53, was issued 17 March, ro9r4,] 


55 


bad 


LIRRAI 


wtiw YC 


; RENE 
QaKkv 


56 


all along the route, and particularly the enthusiastic co6peration 
of botanists in the various regions visited, contributed very 
materially to the success and enjoyment of the trip. 

Although the excursion was formally organized at Chicago, 
before leaving the east a number of short trips were taken to 
localities of botanical interest in the vicinity of New York. 


Te. eal 
Co LAS aA 
i 


¥ 


ot ee 
Pian tea eS 
> = tek IY 


Fic. 1. Map showing route followed by I. P. E. in the United States. 


An afternoon was spent near Hempstead, Long Island, where the 
principal attraction was the peculiar natural prairie described 
by Harper.* To the Europeans, however, the sandy swamps 
proved equally entertaining. A two-day jaunt into southern 
New Jersey afforded an opportunity to study the extensive salt 
marshes about Barnegat and the pine barren flora in the neighbor- 
hood of Warren Grove. In this latter locality the three types 
of vegetation so characteristic of the barrens are well represented, 
viz: the forests of Pinus rigida, Quercus marilandica, etc., the 
pigmy forests of the‘ ‘plains’’—the home of Corema Conradu, and 
and the cedar (Chamecyparis tiyoides) swamps with their unique 
assemblage of rare plants.t A half day each was devoted to the 

* Harper, R. M. The Hempstead Plains of Long Island. Torreya 12: 277— 
286. fig. 1-7. 1912. 

+ For further description, see Stone, W. The plants of southern New 


Jersey, with especial reference to the flora of the pine barrens. Ann. Rept. New 
Jersey State Mus. 1910: 25-828. pl. 1-129 + fig. I-5 + map. 


57 


Brooklyn Botanic Garden and the New York Botanical Garden. 
The beautiful hemlock grove in the Bronx Garden gave the 
visitors their first glimpse of the climax forest of the east. 

Except for a stop at Niagara Falls the journey to Chicago was 
uneventful. Chicago lies in the transition area between the 
forested region of the east and the prairie region of the middle 
west, and the distribution here of forest and prairie is influenced 
largely by edaphic factors. On the uplands forests occupy the 
glacial moraines and the beaches of the former Lake Chicago; 
the rest of the country is grassland.* During the week here 
visits were made to prairies and oak-hickory (Quercus sp., 
Hicoria sp.) forests near the city, to clay bluffs and ravines 
along the lake north of the city, to a tamarack (Larix laricina) 
swamp in northern Indiana, and to a magnificent tract of virgin 
beech-maple (Fagus grandifolia, Acer Saccharum) forest in south- 
ern Michigan—a forest much like those of southern New England 
in its general aspect, but of a more mesophytic type than those 
west of Lake Michigan. The real drawing card in this region, 
however, is the sand-dunes which fringe almost uninterruptedly 
the eastern margin of Lake Michigan, continuing around the 
southern end of the lake and along the western shore as far as 
Chicago. Two entire days were devoted to the study of this 
fascinating area, whose vegetation has been so graphically 
portrayed by Cowles.+ 

The excursionists left Chicago on the evening of August 8, 
and arrived in Lincoln, Nebraska, on the following morning. 
The country about Lincoln is one of rolling prairies with tortuous 
lines of trees fringing the streams. These stream forests, best 
developed on the flood plains, represent the westernmost exten- 
sions of the deciduous forests of the east. Once the eastern 
botanist, westward-bound, has left these behind, he has severed, 
so to speak, the last familiar tie. The prairies themselves in their 
midsummer aspect are depressing. A hasty survey of the region 

* For further discussion see Cowles, H. C. The physiographic ecology of 
Chicago and vicinity. Bot. Gaz. 31: 78-108, 145-182. 1901. 

7 Cowles, H. C. The ecological relations of the vegetation on the sand dunes 
of Lake Michigan. Bot. Gaz. 27: 95-117; 167-202, 281-308; 361-391. fig. I-162. 
1899. 


58 


about Lincoln was made in automobiles, but lack of time and 
intense heat precluded anything resembling careful study. 

That evening the party continued the journey, stopping next 
at Akron, Colorado, 400 miles west of Lincoln. Akron lies in 
the midst of the Great Plains. North and south, east and west, 
as far as the eye can reach, stretches a vast, featureless expanse 
of grassland. Two most interesting days were spent here. The 
first of these was occupied by an eighty-mile automobile ride 
across the plains, to and from the sand hills, with frequent stops. 
The second day was spent about the United States Dry Land 
Experiment Station. The prevalent type of vegetation on the 
plains proper, as contrasted with the sand hills, consists largely 
of various species of Bouteloua, Buchloé, and Aristida, and is 
commonly spoken of as short-grass. The short-grass associa- 
tions, together with those characteristic of the sand hills, have 
been fully discussed by Shantz.* 

Two days were next occupied along the eastern border of the 
Rocky Mountains—at Palmer Lake and near Colorado City— 
studying the vegetation of the tension zone between forest 
toward the west and grassland toward the east. In the invasion 
of grassland by forest the advance guard is usually a thicket in 
which Quercus Gunnisonu. commonly is dominant. The thicket 
stage may be followed by Pinus edulis and Juniperus scopulorum, 
but more often, as in the Garden of the Gods, the two stages are 
telescoped. On the ridges and hills the pinyon and juniper in 
many places are becoming supplanted by Pinus ponderosa 
scopulorum. 

Eight days were devoted to the exploration of the region about 
Pikes Peak, headquarters during this period being at Minne- 
haha-on-Ruxton, about halfway up the cog railway to the 
summit of the peak. Although in certain respects not typical 
of the area as a whole, this region gives one a very fair concep- 
tion of the general nature of the forests of the Rocky Mountains, 
and of the way in which vegetation here is modified as a result of 
differences in exposure and altitude. The climax forest in the 

* Shantz, H.L. Natural vegetation as an indicator of the capabilities of land 


for crop production in the Great Plains area. U.S. Dept. Agr. Bureau of Plant 
Industry Bull. 201. 1911. 


59 


vicinity of Minnehaha (altitude 8,000 feet) consists principally 
of Pseudotsuga taxifolia and Picea Engelmanni. The former 
predominates at lower, the latter at higher elevations. Such 
forests may become quite mesophytic and are best developed on 


Fic, 2. I. P. E. on dunes at Sawyer, Michigan. From left to right: (stand- 
ing) Dr. Brockmann-Jerosch, Dr. E. N. Transeau, Professor H. C. Cowles, Pro- 
fessor O. W. Caldwell, Mr. A. G. Tansley, Dr. O. Paulsen, Mrs. A. G. Tansley, 
Professor C. Schréter, Professor A. Dachnowski, Professor J. M. Coulter, Mrs. H. 
Brockmann-Jerosch, Professor T. J. Stomps, Professor C. von Tubeuf ; (seated) 
Dr. G, D. Fuller, Dr. E. Riibel. Top branches of dune-buried oaks in background. 


north slopes. South slopes, on the other hand, are usually coy- 
ered with a more xerophytic, open type of forest in which Pinus 
ponderosa scopulorum and Pinus flexilis are the characteristic 
trees. Gravel slides in all stages of forestation are a prominent 
feature in the neighborhood of Minnehaha.* The day selected 
for the ascent of Pikes Peak was cold, wet and disagreeable, 

* See Schneider, E. C. The distribution of woody plants in the Pikes Peak 
region. Colorado Coll. Publ., Science Ser. 12: 137-170. Map. i909. Also the 


succession of plant life on the gravel slides in the vicinity of Pikes Peak, loc. cit., 
I2: 289-311. fig. I-6. IgQII. 


60 


and the top of the mountain was covered with snow. Much 
more interesting from a botanical standpoint was the excursion 
up Mount Garfield (altitude 12,365 feet), for which two days 
were set aside. Engelmann spruce continues as the dominant 
tree up to an elevation of about 11,300 feet, where it gives way 
to Pinus aristata, the characteristic timber-line tree. ‘‘ Krumm- 
holz”’ forms of both these trees are common in certain localities. 
On Mount Garfield, as on other peaks of sufficient elevation, 
timber-line as a rule is sharply defined, and the alpine vegetation 
of the rocky meadows above is in marked contrast to that of the 
forests below. The alpine gravel-slides with their curious growth 
of ‘‘cushion-plants’”’ are especially unique. 

The next stopping-place, after leaving Minnehaha, was Salt 
Lake City, Utah, where parts of two days were spent examining 
tracts of vegetation in the proximity of Great Salt Lake. As 
might be anticipated, the natural vegetation of this desert 
country is not very diversified. Sage-brush (Artemisia tridentata) 
dominates nearly everywhere on the fresher soils, while alkaline 
soils are populated by species of Sarcobatus, Kochia, Atriplex, 
and various herbaceous halophytes.* 

The journey from Salt Lake City to Tacoma, Washington, 
was broken by a brief stop at North Yakima, Washington, to 
note the marvelous results that have been achieved in this 
territory by irrigation. Of the six days allowed for western 
Washington, the five spent in the vicinity of Mount Rainier to 
the writer represent the most enjoyable part of the entire trip. 
Two days were devoted to forests in the neighborhood of Kapow- 
sin and the National Park Inn, and two more were spent about 
Camp of the Clouds. Nowhere in the world is there found a 
more magnificent display of coniferous forest than here in the 
Pacific Northwest. The most characteristic tree of the humid 
forests along the western slopes of Mount Rainier, and of the 
lowlands of Washington, is Pseudotsuga taxifolia, which here 
attains enormous dimensions. Associated with this as im- 

* For detailed description of the region visited see Kearney, T. H., Briggs, J. L., 
Shantz, H. L., McLane, J. W. and Piemeisel, R. L. Indicate significance of vege- 


tation in Tooele Valley, Utah. Jour. Agr. Research 1: 365-417. fl. 43-48 + fig. 
I-13 +map. I0914. 


61 


portant constituents of the forest are Tsuga heterophylla and 
Thuja plicata. Among the most conspicuous shrubs in the rank, 
luxuriant undergrowth are Echinopanax horridum, Acer cir- 
cinatum, and Gaultheria Shallon. Seedlings of various trees 
germinate everywhere on fallen logs; there is a wealth of ferns; 
while rocks, ground, logs, and trees are covered with mosses. 

The ecological resemblance between this forest and certain 
forests in the east, e. g., those of northwestern Connecticut, 
is striking. Not only is there a similarity in their general aspect, 
in the mesophytic nature of the undergrowth, etc., but the like- 
ness is further emphasized when a detailed analysis of the flora 
of the two is made. To be sure, the Douglas spruce is lacking in 
the east, beech and chestnut in the west, but hemlock is present 
in both places. Betula lutea is absent from the western forest, 
but Alnus oregana may be considered its ecological equivalent. 
The eastern Acer pennsylvanicum finds its counterpart in the 
western A. circinatum; Taxus canadensis of the east easily corre- 
sponds to T. brevifolia of the west, Cornus Florida to C. Nuttallit; 
and so on. Moreover, many herbaceous species are common to 
both, e. g. Lycopodium lucidulum, Cornus canadensis, Linnaea 
borealis, and Chimaphila umbellata, while the species of Clintonia, 
Trillium, Maianthemum, Tiarella, Oxalis, and other genera 
characteristic of the eastern forest are closely paralleled by very 
similar species here in this western forest. 

Proceeding upward from National Park Inn there is a gradual 
change in the composition of the forest, until at an elevation of 
4,500 feet it consists largely of Tsuga heterophylla, Chamecyparts 
nootkatensis, and various species of Abies. There is no distinct 
timber-line on Mount Rainier. Camp of the Clouds, in the 
Paradise Valley (altitude 5,550 feet), lies in the midst of a lovely 
mountain park where scattered clumps of trees—mainly Abies 
lasiocarpa—alternate with alpine meadows. The meadows below 
the camp are a veritable garden, whose brilliant floral display 
was said by the Swiss members of the party to equal even that 
of their own Alps. 

Returning to Tacoma, some of the party visited the “oak- 
openings”’ in the neighborhood of Spanaway Lake, while others 


62 


took in the kelp-groves near Point Defiance. Further oppor- 
tunity to study the forests of the northwest was given at Medford, 
Oregon, where for three days the excursionists were guests of the 
Medford Commercial and University Clubs. The principal 
attraction here was Crater Lake, situated eighty miles northeast 
of Medford at the crest of the Cascade Mountains, and regarded 
by geologists as one of the wonders of the world. The journey 


Fic. 3. From left to right: Professor C. Schréter, Professor A. Engler, Dr. E. 
Riibel. Photograph taken near Minnehaha by Dr. H. L. Shantz. 


from Medford to the lake was made by automobile. En route, 
there were traversed first the fertile agricultural lands of the 
Rogue River valley (altitude about 1,400 feet), where the natural 
vegetation consists mainly of grassland alternating with oak (Q. 
Garryana, Q. californica) and chaparral. The foothills are 
sparsely timbered with Pinus ponderosa and oak. With increas- 
ing elevation the forest becomes denser, and thirty-five miles 
from Medford the road enters the Crater Lake National Forest, 
which is heavily timbered with Pinus ponderosa, P. Lambertiana, 


63 


Pseudotsuga, and Libocedrus decurrens. At still higher levels 
occur nearly pure growths of Pinus Murrayana, while about 
Crater Lake (altitude 6,000-8,000 feet) are subalpine forests of 
Tsuga Mertensiana, Abies magnifica, A. lasiocarpa, etc. 

Leaving Medford, the party journeyed directly to the Yosemite 
National Park, via San Francisco. Upon entering the foothills 
of the Sierras, after crossing the grassy San Joachim Valley, the 
most striking difference in the vegetation, as compared with that 
farther north, is seen in the presence of Pinus Sabiniana, one of 
the most distinctive Californian coniftrs. The first night in the 
Sierras was spent at El Portal. From here the party traveled by 
stage to the Yosemite Valley, thence to Wawona and the Mari- 
posa big-tree grove. A stop of a day and a half was made here. 
On the return trip to El Portal a night was spent at Glacier Point, 
which commands a splendid view of the Yosemite Valley. The 
chief features of botanical interest in this region are the Sierran 
forests and the big-tree (Sequoia gigantea) groves. Like prac- 
tically all forests west of the Great Plains, those characteristic 
of the high Sierras, and magnificently developed in the vicinity 
of Wawona, are coniferous. The largest and most conspicuous 
tree is Pinus Lambertiana, with which are associated Libocedrus 
decurrens, Abies concolor, Pinus ponderosa, and Pseudotsuga. 
The shrubby undergrowth is mainly chaparral. The big-tree 
occurs in scattered groves, usually intermixed with other trees, 
and only rarely forms pure stands. The excursionists remained 
for the better part of a day in the Mariposa grove, wandering 
about like Lilliputians in the land of Brobdingnag. 

In the vicinity of San Francisco a profitable day was spent on 
Mount Tamalpais with its evergreen-scrub forest of chaparral, 
and in Muir Woods where the acquaintance was made of Sequoia 
sempervirens. 

The objective point of the excursion upon leaving San Fran- 
cisco was Tucson, Arizona. But the thousand-mile railway 
journey was interrupted by several stops, notably at Monterey, 
the home of Cupressus macrocarpa and the center of one of the 
most remarkable communities of endemic plants in existence, 
and at Mecca, where studies were made of succession along the 
margin of Salton Sea. 


64 


So much has been written regarding the vegetation of the 
Tucson region* that it is hardly necessary to attempt any account 
in this connection. During their five days’ stay here the members 
of the party were royally entertained, practically every expense 
being defrayed by the Carnegie Desert Laboratory. Never had 
the writer realized that a desert could be such a congenial habitat. 
The first day was occupied by an examination of the laboratories 
and their environs. On the second the excursionists were driven 
in automobiles eighteen miles across the desert to the foot of the 
Santa Catalina Mountains. That night they encamped in the 
midst of a grove of oaks and junipers 2,500 feet higher and 30 
degrees colder than the distant plain. From this base camp 
trips were made to higher levels. All of the party climbed to 
Bear Canyon (altitude 6,000 feet) and several ascended Mount 
Lemmon (altitude 9,150 feet). 

Two days at the Grand Canyon marked the culmination of 
the I. P. E. From a standpoint of botanical interest the most 
noteworthy feature here is the zonal distribution of the vegeta- 
tion on the sides of the canyon. At the top is an open, park-like 
forest of Pinus ponderosa, P. edulis and Juniperus monosperma. 
Immediately below the rim occur Pseudotsuga and Abies con- 
color, but farther down these are superseded by pinyon and 
juniper. About halfway to the bottom of the canyon is a plateau 
covered with an almost pure growth of Coleogyne ramosissima, 
while at the level of the river vegetation is scant and extremely 
xerophytic, Ephedra sp. being the most characteristic plant. 

Stops for study in the pine forests of eastern Texas and in the 
region about New Orleans had been contemplated, but extensive 
floods made it necessary to abandon this part of the program. 
At New Orleans the party disbanded, most of the European 
members returning to New York via Washington. 


SHEFFIELD SCIENTIFIC SCHOOL, 
YALE UNIVERSITY 


* See especially Spalding, V. M. Distribution and movements of desert plants. 
Carnegie Inst. Publ. No. 113, pp. 1-144. pl. I-3I. 1909. 


65 


LIST OF PLANTS COLLECTED ON THE STEFANSON- 
ANDERSON ARCTIC EXPEDITION, 1908-12 


By P. A. RYDBERG 


A small collection of arctic and subarctic plants was recently 
turned over to me for naming. They were collected rather 
incidentally by Professor R. M. Anderson and kindly donated by 
him to the New York Botanical Garden. One species of Astra- 
galus is probably new and several of the plants are very rare. 
The list is by no means complete as to the vegetation of the 
region, but may be of some interest. 


Smith’s Landing, Slave River, Alberta, June 5, 1908: 


Rosa acicularis Lindl. Small depauperate form. 
Prunus corymbulosa Rydb. In good flowers. 


Bear Rock, mouth of Bear River, Fort Norman, Mackenzie, 
July 9, 1908: 
Cypripedium passerinum Richardson (?). Only in leaf, and the 
species doubtful. 


Mouth of Kogaryuak River, 18 miles east of Coppermine 
River, Coronation Gulf, Arctic coast, Canada, June 18, I9II: 


Salix arctica Pallas. Rather small specimen. 

Draba hirta L. Tall specimen. 

Astragalus sp. An unknown species, somewhat resembling A. 
alpinus, but more slender, with small, narrow, grayish, hirsute 
leaflets, white flowers, purple only on the tip of the keel, 
black-hairy calyx shorter than in A. alpinus. No fruit was 
found, which makes it impossible to characterize the plant 
fully. 

Lupinus arcticus S. Wats. A form more grayish-pubescent than 
the Victoria Island specimen. 

Hedysarum Mackenzit Richards. A low specimen. 

_Rhododendron lapponicum L. 

Casstope tetragona D. Don. Luxuriant specimens. Used as fuel 

by the Esquimeaux. 


66 


Pedicularis lanata Willd. Fair specimen. 
Pedicularis arctica R. Br. Good specimen. 


Southwest Victoria Island, 15 miles east of Point Williams, 
Arctic, Canada, July 21, Igit: 


Salix phlebophylla And. Specimen with rather large leaves. 

Papaver radicatum Rottb. In fruit. 

Dryas integrifolia Vahl. Both the typical and the lobed-leaved 
forms. 

Potentilla pulchella R. Br. Good specimen with rather narrow 
leaf-segments. 

Lupinus arcticus S. Wats. The typical form. 

Maram alpina (L.) Desy. In leaves only. Itis probably the 
red-fruited form. 

Androsace Chamaejasme arctica Kunth. Excellent specimens. 

Statice sibirica (Turcz.) Ledeb. Good specimens. 

Chrysanthemum tntegrifolium Richards. Small specimen. 


Cape Bathurst, Arctic coast, northwest Canada, July 6, 1912: 


Salix anglorum Cham. Typical. 

Oxyria digyna (L.) Compt. Good specimens. 

Ranunculus nivalis L. Good typical specimen. 

Draba glacialis Adams. With young flowers, small-leaved. 

Cochlearia groenlandica L. In flowers. 

Androsace Chamaejasme arctica Kunth. Excellent specimens. 

Primula borealis Duby. Just beginning to bloom, therefore 
pedicels rather short. 

Phlox Richardsonu Hook. Best specimens seen of this rare plant. 

Pneumaria maritima (L.) Hill. Good specimens. 


King Point, Yukon Territory, August 27, I9I2: 


Polygonum fugax Small. Out of bloom and spike gone, but 
probably this species. 

Ledum decumbens Lodd. Small specimen. 

Vaccinium Vitis-Idaea L. Only a fragment. 

Valeriana capitata Pallas. Rather small specimen. 


NEw YoOrRK BOTANICAL GARDEN 


67 


A NEW GENUS FROM MISSOURI 


By KENNETH K. MACKENZIE 


It is a novel experience to receive a specimen from the range 
covered by the Illustrated Flora and by Gray’s Manual which 
cannot be readily referred to well known genera. Not only has 
Mr. E. J. Palmer succeeded in discovering such a plant in south- 
western Missouri, but he has found a plant the family position of 
which may be open to question. I have not been able to find 
anything at all like the plant found by him, and therefore propose 
it as the type of a new genus: 


Geocarpon gen. nov. 


A low glabrous winter-annual branching from the base. 
Leaves opposite, equal or nearly so, entire, sessile and connate at 
base, without stipules, scarcely succulent. Flowers sessile in the 
axils, one at each node, alternating with the flowers above and 
below. Calyx free, somewhat turbinate, the lower third or half 
united into a tube, the segments five, erect, not carinate, un- 
appendaged, ovate, acutish, green with minute white margin, 
not petaloid, 3-nerved, each lateral nerve united below cleft of 
calyx with lateral nerve of next sepal. Corolla absent. Stamens 
five, alternate with calyx lobes, inserted on tube of calyx, the 
filaments white, somewhat flattened, slender, barely 1 mm. long, 
not reaching above calyx, the anthers minute, short oblong, 
bilocular. Capsule ovoid, 1-celled with central placentae, 30-50 
ovuled, dehiscent by three valves, the sharp tips slightly exceed- 
ing the stigmas. Style none. Stigmas three, stigmatose along 
inner surface, alternating with tips of capsule. Seeds minute, 
smoothish, estrophiolate, the slender, straight, ascending funiculi 
remaining attached to the five central placentae. 

G. minimum sp. nov. Branches 1-4 cm. long; leaves of 
branches linear-elliptic to ovate, cucullate, 3-4 mm. long, 1-2 
mm. wide, the basal linear, flat, 4-6 mm. long; calyx 4-5 mm. 
ong, slightly exceeding capsule. 

Type collected by E. J. Palmer (No. 3921) in sandy barrens 


68 


near Alba, Jasper County, Missouri, on April 20, 1913, and sent 
to me by Mr. B. F. Bush for identification. 

This plant is probably to be referred to the family Aizoaceae, 
or as treated in the Synoptical Flora 1: 256 the Ficoideae, and to 
the tribe Aizoideae of that family. In many respects it seems 
to come closer to the genus Cypselea than to any other North 
American genus. It differs markedly in the absence of stipules 
and style and in the capsule not being circumscissile. The other 
genera of the tribe in question, found in this country, are succu- 
lent plants with circumscissile capsules and cornute calyx-lobes- 

The tribe Mollugineae of the same family characterized by a 
calyx divided nearly or quite to the base, and represented in the 
United States by two genera having 3-celled ovaries, is less closely 
related to our plant. Nor can our plant be considered an 
apetalous representative of the Alsinaceae, as the sepals in that 
family are distinct or very nearly so. It seems in fact to represent 
a well-characterized genus. 


NEw YORK 


SHORTER NOTES 


BERGSON AND THE BIOMETRICAL MeEtTHopD. The controversy 
over the definiteness (and fixity) of morphological types is no 
longer of supreme interest to the present-day taxonomists: 
But the exact status of the biometrical method is still under 
discussion; in that connection, at least, it may be interesting to 
note two references from a recent book on philosophy, Bergson’s 
Creative Evolution. They at once support and illumine the 
biometrical method. The first (P. 13) states that ‘‘vital prop- 
erties are never entirely realized, though always on the way to 
become so; they are not so much states as tendencies.”” Because 
of this we have the second statement (P. 116), “the group must 
not be defined by the possession of certain characters but by its 
tendency to emphasize them.” 

JEAN BROADHURST 


69 


PROCEEDINGS On: THE’ CLUB 
JANUARY 13, I914 


The annual meeting of the Club was held on January 13, 1914, 
at the American Museum of Natural History at 8:15 P.M. 
President Burgess presided. Fourteen persons were present. 
The minutes of December 9 were read and approved. 

Mrs. L. N. Keeler, Scarsdale, N. Y. and F. L. Pickett, Indiana 
University, Bloomington, Indiana, were nominated for member- 
ship. The resignations of the following members were read and 
accepted: Mrs. Pamela Eakins, Mrs. George Such, Mrs. Henry 
Dinkelspiel, Mrs. Alice Popper, Miss Mary Brackett, Wm. 
Holmes, and Albert Calman. Mrs. L. M. Keeler and F. L. 
Pickett were then elected to membership in the Club. 

The annual reports of the officers of the Club were next in 
order. The secretary reported that fifteen meetings had been 
held during the year with an average attendance of 15 persons. 
Eleven new members have been elected during the year. Nine 
resignations have been accepted and five deaths have occurred. 
The report was accepted and ordered placed on file. 

The treasurer’s report was presented and upon motion was 
referred to the auditing committee. 

Mr. Norman Taylor, editor of ToRREYA, presented a special 
report relating to that journal. This report was accepted. 

Mr. Sereno Stetson, chairman of the field committee, then gave 
his report and upon motion of Dr. Britton this was accepted and 
a vote of thanks was extended to Mr. Stetson for the work which 
he did in connection with these field meetings. Remarks were 
made by Miss Jean Broadhurst, Dr. Mansfield, Professor Harper 
and others relating to.future field meetings. 

Dr. Britton, chairman of the local flora committee, announced 
that the work on the local flora being prepared by Mr. Norman 
Taylor would be published as a Memoir of the New York Botan- 
ical Garden and goes to press some time in February. Professor 
Harper remarked upon the advisability of continuing the local 
flora work with a special reference to a study of the Cryptogamic 
flora. 


70 


Election of officers for I914 resulted as follows: President, 
Robert Almer Harper; Vice-Presidents, John Hendley Barnhart, 
Herbert Maule Richards; Secretary and Treasurer, Bernard 
Ogilvie Dodge; Editor, Alexander William Evans; Associate 
Editors, Jean Broadhurst, Ernest Dunbar Clark, J. Arthur Harris, 
Marshall Avery Howe, Herbert Maule Richards, Arlow Burdette 
Stout, and Norman Taylor. 

Dr. William Mansfield was elected delegate to the council of 
the New York Academy of Sciences. 


Meeting adjourned. 
MICHAEL LEVINE, 


Secretary pro tem. 


JANUARY 28, 1914 


The meeting of January 28 was held in the lecture room of the 
New York Botanical Garden at 3:30 P.M. Vice-president Barn- 
hart presided. Twenty-five persons were present. The minutes 
of January 13 were read and approved. 

Miss Laura Bragg, Charleston, South Carolina, and Mr. 
Frederick V. Rand, Columbia University, New York City were 
nominated for membership. The secretary then read an applica- 
tion presented by Mr. Norman Taylor for a grant of two hundred 
dollars from the Esther Herman fund of the New York Academy 
of Sciences, to aid him in completing a survey of the Long Island 
flora. This application was unanimously approved. 

Miss Laura Bragg and Frederick V. Rand were then elected 
to membership. 

The announced scientific program consisted of an illustrated 
lecture ‘‘The Coniferous Forests of Eastern North America,’” 
by Dr. Roland M. Harper. The following abstract was furnished 
by the speaker: 

In eastern North America about 30 species of conifers make up 
at least three quarters of the existing forests. Most of the houses 
in the United States and Canada are built of their wood, most 
of our paper comes from the same source, and in some states at 
least, most of the fuel. Most of the conifers grow in pure 
stands of greater or less extent, so that there are about as many 
types of coniferous forest as there are species of conifers. 


Gal 


All but a few of the rarer or less important species were dis- 
cussed from the standpoint of geographical distribution and rela- 
tions to soil, water, climate, fire, etc. Fire as an environmental 
factor has hitherto received scant attention, partly because it is 
commonly regarded as a mere accident, and partly because it is 
not easy to experiment with. But the different species of conifers 
differ widely in their relations to fire, and it seems that for almost 
every type of coniferous forest there is a normal or optimum 
frequency of fire, varying from perhaps once in two or three 
years to once or twice in a century. The paper was illustrated 
_ by 47 lantern slides. 
Meeting adjourned. 
BO. Dope: 

Secretary 


NEWS ITEMS 


William Ruggles Gerard died suddenly in New York City, 
February 26,1914. He was born in Newburgh, N. Y., March 29, 
1841, and in boyhood entered the employ of a druggist in Pough- 
keepsie; he remained in the same business until finally he became 
proprietor of a drug store in that city. He began the study of 
fungi at a time when few American botanists had devoted at- 
tention to that group of plants, his first descriptions of new 
species appearing in the Bulletin of the Torrey Botanical Club 
for October, 1873, before the publication of the earliest myco- 
logical papers of Burrill, Ellis, Farlow, or Morgan. In the 
following year he was one of the founders of the Poughkeepsie 
Society of Natural Science, in whose Proceedings a number of his 
botanical papers were published. In 1877 he removed to New 
York City, where he was an active member of the Torrey Botan- 
ical Club for some years. Before the death of William H. Leggett, 
the founder and editor of the Bulletin, Mr. Gerard was made 
assistant editor, and he followed him as editor, filling that office 
from April, 1882, to December, 1885. In later years he was 
interested in the derivation of plant names, especially those of 


72 


American Indian origin, and contributed papers on this subject 
to Garden & Forest in 1895 and 1896. Otherwise his botanical 
studies seem to have ended with the year 1885. 


Miss Jean Broadhurst has been awarded the degree of Doctor 
of Philosophy by Cornell University and has been appointed 
assistant professor of biology at Teachers College. 


Dr. and Mrs. N. L. Britton and party have returned from bo- 
tanical explorations in Porto Rico. 


We learn from Science that Professor Charles E. Bessey, of the 
University of Nebraska, is spending the month of March at the 
Desert Botanical Laboratory of the Carnegie Institution near 
Tucson, Arizona. Professor Bessey plans to study and collect 
material of numerous species of the desert flora. While he is 
away Dr. R. J. Pool is in charge of the department of botany at 
the University of Nebraska. 


Dr. Simon Schwendener, professor of botany at Berlin, has 
celebrated his eighty-sixth birthday. 


It is stated in Science that Mr. J. Adams, assistant in botany 
in the Royal College of Science, Dublin, has been appointed toa 
position under the Canadian government. 


cA 


_ The T orrey Botanical Club 


Go iibutors of accepted afticles and reviews who wish six 
~ gratuitous copies of the number of Torreya in which their papers 
: appear, will kindly notify the editor when returning proof. 

: Reprints should be ordered, when galley proof is returned 
to. the editor. The New Era Printing Co.; 41 North Queen 
~ Street, Lancaster, Pa., have furnished the following rates: 


es 2pp App 8pp -12pp _—‘ 16pp 20pp 

25 copies $ .75 $1.05 $1.30 $1.80 $2.20 $2.50 
50 copies O02 E20 1.70 2.20 2.50 2.85 
100 copies £152: 25. 155 1.95° 2.55 2.90 3.20 


200 copies —:1.70 2.35 2.90 3.75 4.35 4.70 
~ Covers: 25 for 75 cents, additional covers 1.cent éach. 
-.Plates for reprints, 40 cents each per 100. 


The following Committees have been appointed for 1914 


: Finance Committee Field Committee 
J. H. Barnuart, Chairman SERENO STETSON, Chairman 
Miss.€. C. HAyNEs 
Budget Committee Program Committee 
ee J. H: Barnuart, Chairman Mrs, E. G. Britton, Chairman 
N. L. Brirron Miss JEAN BROADHURST 
B. O. DopcE . C.-StuarRt GAGER 
M. A: Howe EF. J. SEAVER * 
A. W. Evans. 


H. H.. Russy 


Local Flora Committee 


N. L. Britton, Chairman 


Phanerogams: Cryptogams: 
EP. BICKNELL oy Mrs. E.G. BRitTron 
N. L. Brirron ~ - Puitre DOWELL 
eae CO CURTISS: Eeet Tracy E, Hazen 
Ae Ke, KOM ACKENTIE..¢ = M. A. Howe 
* Norman Tayior | W. A. Murrity 


Delegate to the Council of the New York Academy of Sciences 
; WILLIAM MANSFIELD 


OTHER PUBLICATIONS 
OF THE 


TORREY BOTANICAL CLUB 


(1) BULLETIN 


A monthly journal devoted to general botany, established a8 


1870. . Vol. 40 published in 1913, contained 712 pages of text ~ 
and 26 full-page plates. Price $3.00 per annum. For Europe, - 


t4 shillings. .Dulau.& Co., 37 Soho Square, London, are, 3 


agents for England. 
~ Of former volumes, only 24—40 can be supplied entire ; cer- 
tain numbers of other volumes are available, but the entire stock 
of some numbers has been reserved for the completion of sets. 
Vols. 24-27 are furnished at the published price of two dollars : 
each; Vols. 28-40 three dollars each. 
Sine copies (30 cents) will be furnished only wheil not | 
breakine complete volumes. 


(2) MEMOIRS 


The Memoirs, established 1889, are published at irregulas : 
intervals. Volumes I-13 are now completed ; Nos. 1 and 2 of 
Vol. 14 have been issued. The subscription price ts fixed at 
$3.00 per volume in advance. The numbers can also be pur- 


chased singly. A list of titles of the individual ‘papers and of _ 


prices will be furnished on application, 


(3) The Preliminary Catalogue of odnonhyer and Pteri- 
-dophyta reported as growing within one hundred Beige of New 
York, 1888. Price, $1.00. 


Correspondence relating to theabove publications should be — 

addressed to ee ee 
DR. BERNARD O. DODGE 

Columbia University 


New York City — 


Mar 4 oN May, 19014 No. 5 


ORREYA. 


~-A Montuty Journat or Boranicat Notes anp News 


EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


- NORMAN TAYLOR 


JOHN TORREY, 1796-1873 


| ¥ CONTENTS 
4 A Preliminary List of the Lichens Found Within a Radius of 100 Miles of New 
2 York City: G. C. Wood...-:1..--ss0+= pn) SO eS ee STEN eee: Gir ee 73 
‘News Items arth DREAD Sree tae RoR SETS ESIC SS PEPER OETE De CE TICE Cea: REPS Te 95 


_ PUBLISHED FOR THE CLUB 
At 4: Nortu Queen Street, LANCASTER, Pa. 


*) BY THe New Era Printinc Company 


{Entered atthe Post Office at Lancaster, Pa.,as second-class matter.] 


THE TORREY BOTANICAL CLUB 


President 
R. A. HARPER, Pu.D. 


ra 


: Vice Petia 
JOHN HENDLEY BARNHART, A.M., M.D. 
HERBERT M.. RICHARDS, $.D. 


Secretary and Treasurer 


BERNARD O. DODGE, Ph.D. 
Columbia University, New York City 


Editor 


ALEX. W. EVANS, M.D., Px.D: 
Associate Editors 


JEAN BROADHURST, PH.D. : MARSHALL AVERY HOWE, PH.D 


ERNEST D. CLARK, PH.D: : HERBERT M. RICHARDS, S.D, 
J. A. HARRIS PH.D. -\ _AREOW B. STOUT, PH.D. 


NORMAN TAYLOR 


pay 


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NORMAN TAYLOR 


Brooklyn Botanic Garden 
Brooklyn, N. Y. 


TORREYA 


May, Ig1f4. 

Vol. 14 No. 5 
Pei tIMINARY LIST OF TFHE LICHENS FOUND 
WITHIN A RADIUS OF i100 MILES OF 
NEW YORK CITY. 


By GEORGE C. Woop 


Some ten years ago the writer pursued the study of lichens 
with a view to becoming familiar with those forms in the neigh- 
borhood of New York City. A partial list was brought together 
as a result of many excursions and presented to the New-York 
Botanical Garden as part of a work towards an advanced degree 
in science. The list was lost for some years and but recently 
found among the effects of Professor Lucien M. Underwood, then 
in charge of advanced work at the garden. | 

It was thought advisable to publish the list as a beginning of a 
possible future complete survey of the district, particularly with 
a view to its adding some forms to the Long Island biological 
survey, which is being conducted under the auspices of the 
Brooklyn Institute of Arts and Sciences. But the nomenclature 
used in the completion of the list was that of Tuckerman. The 
Engler and Prantl system has since partially superseded it and 
it was thought best to arrange it so that it would meet the new 
requirements.* 


* The following order follows largely the classification set forth by the l’Abbe 
Hue, which is based upon thalline structure. This order does not differ greatfy in 
results from that adapted by Dr. Zahlbruckner in Engler and Prantl, except in a 
few notable instances, though the latter’s is developed upon phylogenetic prin- 
ciples. That lichens are the result of a peculiar parasitic or saprophytic relation 
between a fungal mycelium and an algal host seems a well established fact, but that 
the lichen as a distinct organism has undergone a well marked evolutionary develop- 
ment, is also very evident. Therefore to adopt a classification for them as they 
are, and not because of their origin, is to me the logical course. We have as yet 
no proof of the synthetic formation of lichens im nature. Lichens arise from 
preéxisting lichens and thus probably reproduce only by soredia and fragmenta- 
tion. Protophytic characters are not necessarily to be employed if we wish to 
adopt a natural classification. In rearranging the nomenclature I have had the 
aid in several instances by Dr. H. E. Hasse. 

R. HEBER Howe, JR. 

[No. 4, Vol. 14, of TorREYA, comprising pp. 55-72, was issued 8 April, 1914.] 


73 


74 


The accompanying introductory note by Dr. Howe, curator of 
the Thoreau Museum of Natural History at Concord, Mass., 
fully explains the basis upon which the classification followed 
here is made. The writer wishes to here make public acknowl- 
edgment of the tireless work of Dr. Howe in completely trans- 
posing this entire list from the one system to the other, under 
most unfavorable circumstances. Thanks are also due him for 
reading of the proofs of this article. 

Using Dr. Howe’s transposed list, the writer thought it best 
to use Tuckerman’s nomenclature of families and genera, in so 
far as they fitted into the new scheme as a basis of procedure. 
So far as possible this has been done, the equivalent genus and 
species being placed under the old name following an equality 
(=) sign. In some cases the Tuckerman genus name has been 
dropped entirely in the new scheme. In this case, since there is 
at present no Tuckerman equivalent, the new nomenclature is 
placed first, with the old equivalent of Tuckerman following: 
An asterisk (*) before a genus shows where this plan has been 
followed. Certain new genera indicated in the equivalents have 
also been inserted in the scheme in their proper and relative 
places to give a general idea of the new nomenclature as far as 
represented in this list, and as a sort of cross reference. Such 
genera are indicated by reference to the old Tuckerman genus, 
i. e., Biatorella (see Lecanora). 


FOREWORD 


Not since the year 1823 has a single attempt been made to 
catalogue the lichens growing in the vicinity of New York City. 
It was in that year that Halsey, supplementary to the list 
prepared by Torrey in the year 1819, succeeded in compiling a 
list of some 180 species found or reported to be found within 
a radius of 30 miles of City Hall, New York City. 

Whether it is on account of their lowness in the plant kingdom, 
or of the difficulties attending their study, it is apparent that a 
field, wide and rich in innumerable forms, and entirely free from 
competitors, is open and waiting for one who desires to enlarge 
and enrich the already existing, but meager and scattered data 
concerning the lichen flora of this region. 


i) 


After one and one half years of work, including many thorough 
examinations of the Lichen Herbarium of the New York Botan- 
ical Museum; 30 days spent in the field and much time consumed 
in the identification of species, a list has been prepared comprising 
over 300 species taken from an area included within the limits of 
a circle, the center of which is City Hall, New York City, and the 
radius of which is 100 miles. 

_ This list is by no means complete. Yet I consider it to be a 
beginning large enough to justify me in presenting it at this 
time. It is hoped that many new species, hitherto unknown in 


this locality, together with many new habitats may subsequently 
be added. 
BOUNDARIES 

A circle drawn with its center at City Hall, New York City, 
and having for its radius a line 100 miles in length, will include 
the greater part of Long Island; the whole of Staten Island; the 
greater part of New Jersey; parts of Pennsylvania; New York 
state as far north as Catskill and more than half of Connecticut. 

It has been the custom of the Torrey Botanical Club to include 
within the 100 mile radius all of Connecticut, all of New Jersey, 
all of those counties of Pennsylvania which are touched or crossed 
by the circle, all of Long Island, while the northern boundaries 
of Green, Delaware, and Columbia counties are taken as the 
most northern boundaries of the area situated within the borders 
of New York state. 

This list, however, will include no lichens other than those 
which have been identified as existing strictly within the 100 
mile radius. 

ECOLOGY 


The territory included within the above boundaries is espe- 
cially well adapted for lichen study. It is perhaps as rich in this 
flora as any other area of similar size in the United States. 
District No. 1, including Staten Island, is perhaps most scanty 
in the lichen flora, while the Hudson region, including District 5, 
is very rich in all forms. 

Two leading facts concerning the habitats of lichens make it 
comparatively easy to determine why they are found in abun- 


76 


dance in one place, while scanty or entirely absent in another 
locality. (1) They prefer very moist conditions, and in those 
conditions are almost invariably found upon trees, deadwood, 
rails, or mossy earth. (2) They naturally resist dry conditions, 
but if forced to adapt themselves to such environments are 
almost invariably found on rocks or less frequently upon sterile 
earth. 

It is thus easy to conclude why Staten Island is so scanty in 
forms. It is high and dry, and affords exceedingly few streams. 
If swampy ground occurs, in most cases it is open to the effects of 
the tides, which being saline, preclude any lichen growth. Long 
Island produces a fairly good growth, but almost exclusively 
along its northern shore. This can be explained on the ground 
that (1) its swamps are, in the majority of cases, covered with 
fresh water, (2) and the shore is rocky. (3) It is comparatively 
low. The southern shore, until the extreme eastern end of the 
island is reached, is devoid of varied forms because (1) it is too 
low; (2) it is sandy; and (3) its swamps are lagoons having 
connection with the tides. 

The Bronx and Westchester county are high, dry and rocky. 
Forests are comparatively at a premium. Crustaceous forms are 
the natural result and observation shows that they are practically 
the only forms found there. New Jersey, next to the Highland 
region, shows, perhaps, the most varied flora found within the 
100 mile limit. Here are found many altitudes and as regards 
habitat,—pine barrens, rock deserts, cliffs, swamps and streams. 
Its forms, then, are many and varied, including the crustaceous, 
fruticose, and foliaceous. 

At least one half of the whole number of species enumerated 
in this list are found at or near Closter, N. J., a village situated 
about three and one half miles west of the Palisades and the city 
of Yonkers, N. Y. This village is literally surrounded with 
swamps, which are veritable jungles. Here the foliaceous and 
fruticose forms thrive. A gradual rise toward the Hudson river 
produces varied crustose forms, while the base of the Palisades 
affords many foliaceous as well as crustose forms. Southern New 
Jersey produces a lichen flora comparable to that of Long Island 
as regards its lack of wide range of species. 


uh 


as 


143) 


ses a seme pee 


ee RAN 
© ORANGE om, 


Yee a 


~ 


_| j NCATLANT 16 
; %. tei 
a CRLAN Of, 
S ay 
4 
+ 
DELAWARE % 
BAY 
a cae a [em a or fo 
y 


Map of the Local Flora Range. Only the area within the c| 


ase a 


Eras 


we 


Ny 


NEw) \onoon | 
5 


ne 


SSTeTsoN, 
Orc, 201910 


= 


ircle is covered by this paper. 


et 


The Highland region, comprising District 4, shows the greatest 
_possible range. It includes rocky steeps, mountain brooks, 
torrents, springs and ponds, as well as swampy low ground and 
abundant forests. The Hudson river itself, with its mighty 
evaporation of comparatively fresh water, produces an ideal 
atmospheric condition for the growth of many species. That 
part of Pennsylvania included within these limits, produces by 
far more foliaceous than crustose forks, owing to its peculiar 
atmospheric condition and abundant forests. 

It may be fairly concluded, therefore, that no region could 
afford greater opportunities for the study of lichens, because of 
its great differences in altitudes, soils, and atmospheric condi- 
tions. It consequently follows, that no region of equal area 
produces at the same time such ideal and such poor conditions; 
and so many common and varied forms. 


STATIONS 


The lichens listed are all found in the area composed of the 
above six districts, and are arranged in the order of their im- 
portance and relationships as originally determined by Tucker- 
man. The authority, station, habitat, follow. It will be noticed 
that the station of each district is the one most often mentioned 
in the list. This because all specimens found within a short 
radius of the station are named as at that station. 

It will be noted (see map) that the entire area included within 
the 100 mile radius, has been divided into six districts, each 
having a station, around which all lichens found in that district 
have been grouped. 

District 1—This district comprises all of the county of Rich- 
mond, N. Y., or Staten Island. Richmond, the county seat, is 
the station. 

District 2—This district comprises all that part of Long Island 
west of the 100 mile radius. The station is Cold Spring Harbor. 

District 3.—This district consists of all that part of the state of 
Connecticut within the 100 mile radius. The station is Ellsworth. 

District 4. This district consists of all that part of New York 
state, north of City Hall, New York, and within the 100 mile 
radius. The station is Bronx Park, New York. 


78 


District 5.—This district consists of that portion of the state 
of Pennsylvania within the 100 mile radius and that portion of 
the state of New Jersey, north of a straight line extending from 
Perth Amboy southwest to Trenton. The station is Closter. 

District 6.—This district consists of all that part of the state 
of New Jersey south of a straight line extending from Perth 
Amboy southwest to Trenton and north of the 100 mile radius. 
The station is Newfield. 


AUTHORITIES 


Tuckerman is held as the authority in compiling this list for 
various reasons, the most important of which are the following: 
(1) He was and is our foremost American authority. (2) He 
was thoroughly conversant with American forms and conditions. 
(3) His descriptions, though from some standpoints obscure, are 
much clearer in their application to American lichens than those 
of European authorities. For purposes of comparison, the speci- 
mens in the herbarium of the New York Botanical Garden were 
accepted as correctly identified, only on such good authority as 
that of Leighton, Willey, Miss Clara Cummings, and Bruce 
Fink. 

All recent and accepted changes in nomenclature occurring 
since the death of Tuckerman are included. Several genera 
(Acolium, Graphis, Calicium, etc.) have been identified under 
other authorities, principally Nylander and Fries. 


ABBREVIATIONS 


In preparing a list of this length, many repetitions necessarily 
occur, as regards stations, habitat, and authority. Conse- 
quently, after their first insertion, such are abbreviated. 


I. Order: GYMNOCARPI (Schrad.) Fr. 
= GYMNOCARPALES (Luyken) Fr. 
Sub-order: CYCLOCARPINEAE (Wain). 
I. Group: RADIATAE Hue 


Family 1. Usneei = Usneaceae Eschew. 


Genus 1. Usnea barbata (L.) Fr. Closter, N. J. Common. trees. 
= composite material. 


U. longissima Ach. Ocean, N. J. t. 
U. angulata Ach. Palisades, N. J.; C. t: 
U. barbata ceratina Schaer. Atco, N. J., May’s Land- 
= plicata (L.) Web. ing, Closter, N. J. lfc 
U. barbata plicata Fr. Camden, N. J.; C. (e 
=plicata var. Huei (Borst.) 
Howe. 
U. barbata dasypaoga Fr. Camden, N. J.; C. te 
= barbata (L.) Web. 
U. barbata florida Fr. Gamden> Nee; Co € te 
= florida (L.) Web. 
U. barbata hirta Fr. (Cx (bs 
= floridaf. hirta (L.) Ach. 
U. barbata rubiginea Michx. Philaz Pa. (€: t. 
= florida ft. rubiginea 
Michx. 
U. trichodea Ach. Otter Pond, N. J., Young; 
Orient, L. I. sige 
Genus 2. Evernia furfuracea (L.) Mann. C.; Catskill, N. Y. le 
= Parmelia furfuracea (L.) 
Ach. 
E. furfuracea Cladonia Tuck. C. t. 


= Parmelia furfuracea var. 
Cladonia (Tuck.) Howe. 


E. trunastri (L.) Ach. Cat.; Ellsworth, Conn. t. and 
= Letharia thamnodes (Flot. ) fences. 
Hue. 
Genus 3. Ramalina calicaris (L.) Fr. C.; Summit Mt., N. Y.; 
= composite. Peach Bottom, Pa. 
Common. t. and 
rocks 
R. calicaris canaliculata Fr. C.; Summit Mt., N. J. te 
= canaliculata (Fr.) Herre. 
R. calicaris farinacea Schaer. C. t. 
= farinacea (L.) Ach. 
R. calicaris fastigata Fr. & tie 
= fastigiata (Per.) Ach. 
emend. 
R. calicaris fraxinea Fr. Phila. t 


= fastigata var. subam- 
pliata (Nyl.) Howe. 


R. rigida (Ach.) Pers. ING Ve City7 Atco; N- J-; 
= Urlleyi Howe. Camden, N. J. t. 
Genus 4. Alectoria jubata (L.) Ach. (Ge t. 
= composite 
A. jubata implexa Fr. Cc: earth. 


= jubata var. implexa 
(Hoffm.) Fr. 


Genus 5. 


Genus I. 


Genus 2. 


80 


A. jubata chalybeiformis Ach. C.; Jamaica, L. I. earth and 
= chalybeiformis (L.) S. F. firs 
Gray. 

A. jubata bicolor Fr. Susquehanna, Pa. earth 
= bicolor (Ehrh.) Nyl. : 

A. ochroleuca (Ehrh.) Nyl. Susquehanna, Pa. e: 

Telochistes chrysopthalmus (L.) 

Norm. C. Greenpoint, L. I.; 
Phila.; Vineland; Cam.., 
N. J. Common. r. 
2. Group: RADIATI-STRATOSI Hue 
Family 1. Cladoniei = Cladoniaceae 

Stereocaulon denudatum Floerk. C.; Pal. rocks 

S. paschale (L.) Ach. Pal.; Sus. e., r 

S. tomentosum Fr. C. e. 

Cladonia rangiferina alpestris 
Wg C.; Ja. logs. 
= alpestris (L.) Rabenh. 

C. rangiferina sylvatica L. C.; Staten Id.; Ells. e. 
= sylvatica Hoffm. 

C. papillaria (Ehrh.) Hoffm. C.; Cat.; Pt. Jefferson, 

INANE gravelly 
earth. 

C. macilenta Hoffm. (Ehrh.) C.; Pal.; Ja.; Ells. Com- 

mon. logs. 

C. cornucopioides (L.) Fr. C.; Fhila.; Richmond 
= coccifera (L.) Willd. Hill, L. I.; Pal.; Ells. e. 

C. coccifera (Schaer.) Spic. G& stumps, e. 

C. bellidiflora (Ach.) Schaer. Princess Bay, St. Id. e 

C. cristatella Tuck. Rich. Hill, Phila.; Todt 

Hill, St. Id.; Richmond, 
St. Id.; Princess Bay, 
St. Id. Common. Gop Es 

C. lepidata Fr. G 
= C. cristatella var. ochro- 
carpia Tuck. 

C. uncialis (L.) Web. C.; Rich.; Ridgewood; 

Bridgeton, N. J. 

C. uncialis adunca Ach. (OF 
= uncialis (L.) Web. 

C. furcata (Huds.) Schaer. jenn (Ce e. 

C. fimbriata adspersa Tuck. C; e. 
= C. furcata var. scabriu- 
scula (Del.) Coem. 

C. furcata racemosa (Hoffm.) 

Fl. GeNE Yo G3 Ells: é. 


C. furcata subulata F\. 
= v. palamaea (Ach.) Nyl. 


C.; Pal.; Pt. Jeff. 


Genus 3. 


81 


C. furcata crispata F1. 
= crispata (Ach.) Flot. 
C. squamosa (Scop.) Hoffm. 


C. Botryella Nyl. =? 

C. caespiticia (Pers.) FI. 

C. squamosa delicata Fr. 
= delicata (Ehrh.) Fik. 

C. turgida (Ehrh.) Hoffm. 

C. mitrula Tuck. 


C. gracilis symphiacarpa Tuck. 


= subcariosa Nyl. 
C. cariosa (Ach.) Spreng. 


C. pyxidata symphicarpia Nyl. 
= alpicola 
Wain. 

C. decortica (Floerk.) Spreng. 

C. gracilis elongata (Jacq.) 
Flk. 

C. gracilis hybrida Schaer. 


var. Karelica 


= var. chordalis (Floerk.). 
C. cornuta (L.) Schaer. 


C. degenerans (Floerk.) Spreng. 


C. verticillata evoluta Fr. 
C. gracilis verticillata Fr. 

= verticillata Hoffm. 
C. pyxidata (L.) Fr. 


C. fimbriata (L.) Fr. 
C. fimbriata tubaeformis Fr. 


= var. simplex (Weis.) Flot. 
Baeomyces aeruginosus (Scop.). 


IDKE. 
= Icmadophila 
(L.) Zahlbr. 
B. byssoides (L.) Schaer. 


ericetorum 


B. roseus Pers. 


B. icmadophilus Nyl. 
= Icmadophila 
(L.) Zahlbr. 


ericetorum 


ce e. 
(C e. 
C.; Flushing, L. I. decayed 
logs. 
INS WK ES e. 
Tarrytown, N. Y.; Ja. ie: 
(e, wood. 
Cc e. 
C.; Pal.; N. Y. C.; Green- 
wood Cem., Bklyn. 
Common. 
G: 
GE Venviss NeYesIN= Ye 
City; Todt H. Common. e. 
@Cate- Pils: e. 
Ja. e. 
@ e. 
G3) Cats: r., logs. 
GC: e. 
G: e. 
Ja. e. 
C.; Ells. e. 
3 Oysters Bay, 1.1: 
St. Id.; Safe Harbor, 
site li¢hs JPmvikins Iie 
common. e. 
Cras Rich.-aeale e., logs. 
Ja. e 
C.; Summit Lake, N. J. decaying 
wood. 
INE ve: decaying 
wood 
Ce odtaa Le evalley, 
Stream, I, i: Law- 
rence, L.I. Common. e. 
St. Id.; Shelbourne, N. 
Wa e. 


*Genus I. 


Genus I. 


Genus 2. 


Genus 3. 


82 


3. Group: STRATOSAE Hue. 


Family 1. Pseudophyciaceae 
Pseudophyscia comosa 
(Eschw.) Nyl. & Cam. 
= Anaptychia comosa 
(Eschw.) Mass. 


P. aquila (Ach.) Hue New Lots, L. I. 
= Physcia aquila (Ach.) 
Nyl. 


P. aquila var. detonsa Tuck. PalnG€: 
= Physcia aquila detonsa 
Tuck. 
P. aquila detonsa (Tuck.). Pal. 
= Physcia detonsa Fr. 
P. speciosa (Wulf.) Miill. Ce als 
= Physcia speciosa (Wullf.) 
(Ach.) Nyl. 
P. speciosa var. galactophylla 
Tuck. (& 
= Physcia speciosa galacto- 
phylla (Tuck.). 
P. hypoleuca (Muhl.) Hue. C.; Cam.; Atco; Flush- 
= Physcia hypoleuca ing, L. I. 
(Muhl.) Tuck. ; 


Family 2. -Physciaceae 
Physcia hispida (Schreb.) Fr. ‘C. 
= tenella (Scop.) Nyl. 


P. tribacea (Ach.) Tuck. R. Hill.; C., common. 
P. stellaris (L.) Nyl. St. Id.; C.; Pal. Common. 
P. pulverulenta (Hoffm.) Nyl. Cam.; Cat.; C.; Atco. 
P. obscura (Ehrh.) Th. Fr. C.; Cam.; Rich.; Cold 
Spring Harbor, L. I. 
P. obscura endochrysea Nyl. ye Camr 
= var. endococcina (Koeb.) 
Th. Fr. 
P. adglutinata (Floerk.) Nyl. C. 
Pyxine cocoes (Sw.) Nyl. C.; Pal.; Cen. Park, N. Y.; 
Cam. 
P. sorediata (Ach.) Fr. C. 
Xanthoria parietina (L.) Th.Fr. Flatbush; Flushing; C.; 
= Telochistes parietinus Ridgewood, L. I. 
(L.) Norm. 
X. lychnea (Ach.) Th. Fr. St. Id.; C.; Flatbush, 


= Telochistes lychneus Nyl. INDY. 
X. polycarpa (Hoffm.) Th. Fr. C.; Cam. 

= Telochistes polycarpus 

(Ehrh.) Tuck. 


Genus I. 


Genus 2. 


*Genus I. 


*Genus 2. 


85 


Family 3. 


Buellia stellulata (Tayl.) 
Mudd. 

B. spuria (Schaer) Korb. 

B. dialyta (Nyl.) Tuck. 

B. parasema (Ach.) Koerb. 
= Lecidea parasema Ach. 

B. myriocarpa (Ach.) Mudd. 
= Buellia myriacarpa (D. 
C.) Mudd. 

B. Schraeret De Not 

B. petraea (Flot. and Koerb.) 
Tuck. 
= Rhizocarpon petraea 
(Wulf.) Mass. 

B. petraca Montagnei Tuck. 

B. Elizae Tuck. 

B. lactea Mass. 
= Polyblastea lactea (Mass.) 
Korb. 


Buelliaceae 


C: 
Ce 
C 
E 
Cc: 


(C. 
C.; Sus. 
(Coe Sie 


New Bedford, Ct. 
Ce Pal: 


B. pullata Tuck. IPE, [ei 
B. vernicorna Tuck. Cc 
Rinodina constans Nyl. (A 
= Maronea constans Zw. 
R. Ascociscana Tuck. Sus. 
R. sophodes (Ach.) Th. Fr. (Ce 
R. sophodes confragosa Nyl. (Ce 
= R. confrogosa (Ach.) 
Koerb. 
Family 4. Caloplacaceae 
Blastema ferrugineum (Huds.) 
Arn. C 
= Placodium ferrugineum 
(Huds.) Hepp. 
B. ferrugineum nigrescens 
(Tuck.) (e; 
=P. ferrugineum nigres- 
cens (Tuck.) Fr. 
B. rupestris (Scop) Zahlbr. INfe We (C 
= P. rupestre (Scop.) Br. 
and Rostr. 
Caloplaca aurantiaca (Lightf.) 
AM; Ir 35 Rich: 


= Placodium aurantiacum 
(Lightf.) Naeg. and Hepp. 
P. cerinum (Ehrh.) Zahlbr. 


C. Common. 


ee Ganwe 


tite 
teas 
r., fence. 


Ee Genwe 


tae ewe 


d. w. 


*Genus I. 


*Genus 2. 


* Genus 3. 


Genus 4. 


84 


C. aurantiaca erytheilum (Ach.). C. 
= P. aurantiacum erythel- 
lum Ach. 

C. cinnabarina (Ach.) Zahlbr. 


= P. cinnabarinum (Ach.) Id. 
Anz. 
Family 5. Parmeliaceae 
Platysma glaucum (L.) Nyl. Bergen Co. 
=Cetraria glauca (L). 
Ach. 
P. lacunosum var. Atlanticum 
(Tuck.) Nyl. C3" Ja; Cold) ‘Spring 
= C. lacunosa Ach. Harbor, L. I. 


C.; Ft. Wadsworth, St. 


P. aurescens (Tuck.) Nyl. 
= C. aurescens Tuck. 
P. lepatizon (Ach.) Wain. 


Passaic, IN, Joe (C.e (C2 S; 


ile 
C.; Del. Water Gap, Pa. 


=C. Fahlunensis (L.) 


Schaer. 
P. juniperina (L.) Nyl. (CS 
= C. juniperina (L.) Ach. 
P. juniperina var. Pinastri 
(Ach.) Nyl. Bergen Co. 
=C. juniperina Pinastri 
Ach. 


P. Fendleri (Tuck.) Nyl. 
= C. Fendleri Tuck. 

P. Oakesianum (Tuck.) Nyl. 
= C. Oakesiana Tuck. 

P. Islandica (L.) Ach. 
= C. Islandica (L.) Nyl. 


C.; Cam.; Atlantic, N. J. 


Cat. 


Ulster Co., N. Y.; Rich. 
Hill, Del. Water Gap. 
Common. 

Nephromopsis ciliaris (Ach.) 


Hue. C.; East N. Y.; Brainerd, 


= C. ciliaris Ach. Ct. Common. 
Anzia colpodes (Michx.) Stizb. At., Bergen Co. Com- 
mon. 
= Parmelia colpodes (Ach.) 
Nyl. 
Parmelia caesia Fr. (Ce 
= Physica caesia (Hoffm,) 
Nyl. 
P. crinita Ach. C.; Ridg.; Ber. Co. 
P. cetrata Ach. =? At. 
P. laevigata (Sm.) Nyl. =? Ocean, N. J.; Monmouth, 
IN do 
P. pertusa (Schrank) Schaer. Ber. Co.; Oc. 


(Ach.) Nyl. 


fences. 


*Genus 5. 


*Genus 6. 


*Genus I. 


*Genus 2. 


Genus 3. 


85 


P. olivacea (L.) Ach. 
P. Borreri Turn. 


. Borreri rudecta Tuck. 
. caperata (L.) Ach. 
. conspersa (Ehrh.) Ach. 


ne} re) Se) 


P. saxitalis (L.) Fr. 

P. saxitalis sulcata (Tayl.) 
Nyl. é 

P. tiliacea (Hofftm.) Flk. 

P. perforata (Jacq.) Ach. 


P. perlata (L.) Ach. 
= olivaria (Ach.) Hue 
P. physodes (L.) Ach. 
P. centrifuga (L.) Ach. 
Parmeliopsis aleurites (Ach.) 
Nyl. 
= Cetraria aleurites (Ach.) 
Th. Fr. and Parmelia aleu- 
rites Nyl. 
P. placorodia Ny). 
= C. placorodia Nyl. 
P. ambigua (Wulf.) Ach. 
= Parmeliopsis ambigua 
Candelaria concolor (Dicks.) 
Arn. 
= Telochistes concolor 
(Dicks.). 


C Cam 

(C25 LBirie Se licks Cone 
anus; Flatlands, Glen 
Cove, L.I. Common. 

CsStealas 

C.; Pal. Common. 

C.; St. Id.; Prospect Pk., 
B’klyn; Ridg.; Pater- 
son, N. J. Common. 

C.; Ridg.; Bra.; Val.; St. 


(On S, dele 

C.; Val. St. Common. 

Cia Rich! Rides Git— 
fords, St. Id. 

Cl Ss. He-Ridgs- Vale 
St. 


Oc.; Monmouth, N. J. 


C.; Valley Stream, L. I. 


CiGampe-wRich=1Stlde 


Family 6. Lecanoraceae 


Candelariella vitellinum 
(Ehrh.) Muhl. Arg. 
= Placodium vitellinum 
(Ehrh.) Naeg. and Hepp. 
Icmadophila ericetorum (L.) 
Zahlbr. 
= Baeomyces aeruginosus 
(Scop.) D. C. 

I. ericetorum Nyl. (Zahlbr.) 
= B. icmadophilus Ny]. 
Lecanora fuscata (Schrad.) 

ADjoke 1Bree 
= Acarospora fuscata 
(Schrad.) Arn. 


Rich.; Bay Ridge, L. I. 


C.; Sum. Lake; N. J. 


St. Id.; Shelbourne, N. 
Ve. 
Chester, N. J. 


es Ge 


Genus I. 


86 


L. tartarea (L.) Ach. 
= Ochrolechia tartarea (L.) 
Mass. 

L. varia (Ehrh.) Nyl. 


L. varia saepincola Fr. 
L. atra (Huds.) Ach. 
L. Bockit (Fr.) Th. Fr. 

= L. gibbosa (Ach.). 
L. muralis (Schreb.) Tuck. 
L. xanthophana Nyl. 
L. pallescens (L.) Schaer. 
= Ochrolechia pallescens (L.) 
Mass. 
pallida (Schreb.) Schaer. 
rubina (Vill.) Wain. 
subfusca (L.) Ach. 
pallida cancriformis Tuck. 


Satan 


= L. albella v. cancriformis 
(Tuck.) Herre. 
L. allophana Nyl. 
L. subfusca distans (Ach.) Nyl. 
L. Hageni Ach. 
L. Willeyi Tuck. 
L. Cupressi Tuck. 
L. orosthea (Sw.) 
= Lecanora symmicta Nyl. 
L. athroocarpa (Dub.) Nyl. 
= Lecidea athroocarpa 
Ach. 
L. cinerea Ach. 
L. lacustris (With.) Nyl. 


L. cervina (Pers.) Nyl. 
= Acarospora chlorophana 
(Walbg.) Mass. or =A. 
squamulosa (Schrad.) Th. 
Fr. 
L. cervina discreta Nyl. 
= A. discreta (Ach.) Th. Fr. 
L. privigna Nyl. 
= Biatorella simplex (Dav.) 
Br. and Rostr. 


Family 7. 
Pertusaria multipuncta 
(Turn.) Nyl. 
P. globularis Ach. 


C.; Ells.; Pal. 


C.; Ridg.; Glen Cove, 
ites 

C.; Ridg. 

Poestenkill, N. J. 

Grea 

(Co 

(Gop lel 

C.; Pal. 


C.; Ridg.; Flat.; Val. St. 
Haverstraw, N. Y.; Sus. 
At.; Val. St.; Rich. Hill. 
C. 

Rich. Hill. 


(ee 
Cc. 
C; 
G: 
(Cr 
C. 


Cleat 


Pertusariaceae 


(Ce 
(O53 (Cale, 


e., r 

tous 

Gases 

te 

I. 

it 

Bon Gly Vii 

Ep 

iP 

t2,. 1s 1deawe 

tr., rails. 

ts 

Gi eTie 

(Gaemls. 

i., fences. 

(Ec 

ite 

t. 

sandstone. 

r. under 
water 

ig 

ifs 

ie 

ts 

tion 


Genus I. 
Genus 2. 


Genus I. 


Genus 2. 


Genus I. 


Genus 2. 


Genus I. 


87 


P. velata (Turn.) Nyl. 

P. communis DC. 

P. leioplaca (Ach.) Schaer. 
P. pustulata Duby. 


@yaRads: 

Ge Sie lds Rade. 
(es 

(Cus ane Tallin 


P. glomerata (Schleich.) Schaer. Ja. 


P. Wulfenii (DC.) Fr. Cat. 
Family 8. Acarosporaceae 
Biatorella (see Lecanora). 
Acarospora (see Lecanora). 
Family 9. Stictaceae 

Sticta crocata (L..) Ach. Cc. 
S. quercizans (Michx.) Ach. @ Pall Sus: 

= Lobaria quercizans 

Michx. 
S. pulmonaria (L.) Ach. C.; Pal. Common. 


= Lobaria pulmonaria (L.) 
Hoffm. 

S. amplissima (Scop.) Mass. 
= Lobaria amplissima 
(Seop.) Arn. 


S. aurata (Sm.) Ach. 


Pale-aNe Wotss Ney eC: 
Newfield, N. J.; Mata- 
moras, Pa.; Safe Har- 
bor, Pa. Common. 

Gloucester, N. J. 


S. sylvatica (Huds.) S. F. Gray. Cat. 
Lobaria (see Sticta). 

Family 10. Peltigeraceae 
Peltigera venosa (L.) Hoffm. c: 


P. canina (L.) Hoffm. 
P. canina spuria Ach. 

= P. spuria (Ach.) DC. 
P. apthosa (L.) Hoffm. 


P. korizontalis (L.) Hoffm. 
P. polydactyla (Neck.) Hoffm. 
P. rufescens (Sw) Hoffm. 
Nephroma tomentosum 


Ce Pal alas ias 

C., Glou.; Old Fields, N. 
Ve 

C.; Phila.; Bra.; Peek- 
skill; Fishkill. 

(Cue lee, 

sus 

C.; Newf.; Glou., N. J 


(Hoffm.) Koerb. C. 
N. Helveticum Ach. (E28 (CHie, 
N. laevigatum Ach. C.; Cam.; At. 
Family 11. Pannariaceae 
Pannaria try plophylla (Ach.) 
Mass. Newf. 


= Parmeliella tryptophylla 


Miill. Arg. 
P. molybdaea (Pers.) Tuck. 
= Collema molybdium 


Newf.; C.; Salem; Hack- 
ensack, N. J. 


ibe, 
(Bion 
bon 


ne aats” 


mosses. 


T., 


I. 
Yr. 
Yr. 


r. in 


(fo 


ota Wein pe ta} 


Genus 2. 


Genus 3. 


Genus 4. 


Genus I. 


Genus 2. 


Genus I. 


88 


P. molybdaea cronia Nyl. 
= Collema molybdium var. 
cronia (Nyl.). 
P. languinosa (Ach.) Koerb. 
P. byssina (Hoffm.) Tuck. 
= Dichodium byssinum 
(Ach.) Nyl. 
P. nigra (Huds.) Nyl. 
= Placythium nigrum 
(Huds.) S. Gray. 
P. rubiginosa (Thunb.) Delis. 


P. leucosticta Tuck. 


P. microphylla (Sw.) Delis. 
P. lurida (Mont.) Nyl. 

= Physma lurida Mont. 
Hydotheria venosa Russ. 
Parmeliella (see Pannaria). 
Placyrthium (see Pannaria). 


Family 12. 


Gyrophora (see Umbilicaria). 

Umbilicaria vellea (L.) Nyl. 
= Gyrophora (L.) 
Ach. 

U. Dilleni Tuck. 
= G. Dilleni (Tuck.) Mil. 
Arg. 

U. Muhlenbergit (Ach.) Tuck. 
= G. Muhlenbergiit (Ach.) 
Schneid. 

U. papulosa Tuck. 
=U. pustulata papulosa 
Tuck. 

U. pustulata (L.) Hoffm. 


vellea 


U. Pennsylvanica Hoffm. 
U. hirsuta (Ach.) Stenh. 
= G. hirsuta (L.) Ach. 


Family 13. 
Lecidea contigua Fr. 
L. enteroleuca Ach. 
L. granosa Tuck. 
= Toninia granosa (Tuck.). 
L. tessellina Tuck. 


Sus. 


C.; Pal. 
C.; Cam.; Hack. 


C.; Hack. 


Newf.; Ulster Co., N. Y.; 
Shadaken, Pa. 
C.; Newf.; Weehawken, 


N. J. 

Cc. 

C.; Pal.; Cam.; At.; N. 
Y.C.; Newf. 


C. V. under water. 


Gyrophoraceae 


Cc: 


Sus. 


C.; Sus. 


Rockland Co. 


Garrison’s; Washington 
Heights, N. Y. C.; 
‘Morris Pond, N. J. 

Sus.; Mat.; Pa. 

Cat. 


Lecidiaceae 


C.; St. Id.; Ja. Common. 
(Cu8 Cait. 
Ce 


C. 


ete 
ae 


a 


., bricks. 


89 


L. albocoerulescens (Wult.) 


Schaer. R. Hill, West Graham, 
Ce r. 
L. muscorum Koerb. G r. 
= Bacidia muscorum (Ach.) 
Mudd. 
L. alba (Schl.) Nyl. = ? St. Id. ite 
L. elaeochroma Tuck. (e 165 


= Lecidea parasema v. ela- 
eochroma (Tayl.) Ach. 


L. spilota Fr. CG Ic 
= Lecidea tessellata Fek. 

L. lutea Schaer. Newf. it 
= Biatorina lutea (Dicks.) 
Arn. 


Genus 2. Psora (see Biatora). 
Genus 3. Catillaria (see Biatora). 
Genus 4. Biatorina (see Biatora). 


Genus 5. Biatora anthracophila Nyl. Cc; pine wood. 

= Lecidea anthracophila 
Nyl. 

B. campestris Fr. Cr erat e. 
= Biatorella campestris 
(ire) Iai, Iie. 

B. chlorantha Tuck. Cart: pine wood. 
= Bacidia chlorantha 
(Tuck.) Fink. . 

B. chlorosticta Tuck. Cc cedar bark. 
= Bacidia chlorosticta 
(Tuck.). 

B. cuprea (Sommerf.) Fr. Pine Is.; N. Y. cedar bark. 
= Lecidea cuprea 
Sommerf. 

B. geophana Nyl. ec e: 

B. granulosa (Ehrh.) Poetsch. Todt Hill, St. Id. sand. 
= Lecidea granulosa (Ehrh.) 
Schaer. 

B. cupreo-rosella Ny. Orange Co., N. Y. ie 
= Bilimbia cupria Mass. 

B. exigua (Schrad.) Ach. (Ce r. 
= Rinodina exigua (Ach.) 
IMs Iie 

B. hypnophila Turn. (Ce trop, Gla Atv 
= Bilimbia hypnophila 
(Ach.) Th. Fr. 

B. icteria Mont. orale e. 


= Psora icteria (Mont.) 
Fink. 


90 


B. mixta Fr. - 1emill. 
= Biatorina mixta (With.) 
Fink. 

B. parvifolia (Pers.) Tuck. Ce 
= Lecidea parvifolia (Pers.) 

Nyl. 


B. rubella Fr. C.; Pal.; Newf. 


= Bacidia rubella (Hoffm.) 
Mass. 

B. Russellit Tuck. C.; Sus. 
= Psora Russelliit (Tuck.) 
Fink. 

B. Resinae Fr. GC: 
= Biatorella resinae (Fr.) 

AN Jie 

B. rufo-nigra Tuck. Pal. 
= Lecidea rufo-nigra 
(Tuck.) Hasse. 

B. russula (Ach.). CG: 
= Biatorina russula Ach. 

B. sanguineo-atra (Fr.) Tuck. C. 
= Bacidia atrasanguineo 
(Schaer.) Th. Fr. 

B. suffusa Fr. C- 
= Bacidia fuscorubella v. 
suffusa (Fr.) Fink. 

B. uliginosa (Schrad.) Ach. « C. 

= Lecidea uliginosa (Schrad.) 
Ach. 


B. umbrina Ach. (es 
= Bacidia umbrina (Ach.) 
Br. et Rostr. 
B. varians Ach. C.; common. 


= Lecidea varians Ach. 
B. vernalis (L.) Fr. (Cs, Cai. 
= Lecidea vernalis (L.) Ach. 
B. viridescens (Schrad.) Fr. Cc: 
= Lecidea viridescens 
(Schrad.) Ach. 


B. Schweinitzii Fr. C.; Newf. 


= Bacidia Schweinitzii 
(Tuck.) Fink. 


B. inundata Fr. G: 
= Bacidia inundata (Fr.) 
Koerb. 

B. fossarum (Duff.) Mont. C. 


= Biatorella fossarum 
(Duff.) Th. Fr. 


white pine. 


rotting log; 


e. 
r., rails. 
bor, ls SY 
its 
rotting 
wood. 
rotting 
wood. 
rotting 
wood. 
ts 


Genus 6. 
Genus 7. 
Genus 8. 
Genus 9. 
*Genus 10. 


*Genus I. 


*Genus 2. 


Genus I. 


oi 


B. nigra Tuck. GE: 
=? 
B. decolorans (Hoffm.) Fr. (Cz 


= Lecidea decolorans 
(Hoffm.) Schaer. 

B. tricolor With. (ee 
= catillaria tricolor, (With). 
Adios Ihe 

B. denigrata Fr. Ce. 
= Biatorina synothea,(Ach.) 
Koerb. 

B. fusco-rubella Hofim. & 
= Bacidia fusco-rubella 
(Hoffm.) Arn. 

Bacidia (see Biatora). 

Bilimbia (see Biatora). 

Toninia (see Biatora). 

Rhizocarpon (see Buellia). 

Lopadium vulpinum (Tuck.). 
= Heterothecium vulpinum 
Tuck. Atlantic Co., N. J. 

L. pezizoideum (Ach.) Koerb. 
=H. pezizoideum (Ach.) C. 
Flot. 


Family 14. Diptochistaceae 


Conotrema urceolatum (Ach.) 


Tuck. CaWaleSt: 
= Gyrostomum urceolatum 
Fr. 
Diplochistes scruposus (L.) 
Norm. (Cz 
= Urceolaria scruposa (L.) 
Nyl. 


Family 15. Graphidaceae 
Graphis scripta (L.) Ach. Gy Nees C2 Rich=) Git= 
fords, St. Id.; Conewa- 
go, Pa. Common. 


G. scripta graciliens Nyl. C. S. Harbor. 
G. scripta f. recta Nyl. CG Raleaoteld: 
G. scripta assimilis Nyl. Cc 

G. erumpens Nyl. Giff. 

G. elegans (Sm.) Ach. Cy 

G. dendritica Ach. Gi Pal: 


= Phaeographis dendritica 
(Ach.) Miill. Arg. 
G. sculpturata Ach. (Ce 


fir bark. 


Aeon o a8 


Genus 2. 
Genus 3. 


Genus 4. 


Genus I. 
Genus 2. 


Genus I. 


92 


Phaeographis (see Graphis). 
Opegrapha varia Pers. 


O. varia rimalis Fr. 

O. vulgata Ach. 

O. viridis Pers. 

Xylogropha parallela (Ach.) 
Fr. 


C. Newf.; St. Id.; Rich. 


Hall Wt 


(Ce 
c: 
Cc 


Lakewood, N. J. 


Family 16. Arthoniaceae 


Arthothelium (see Arthonia). 
Arthonia glaucescens Nyl. 
A. lecidella Nyl. 
A. astroidea Ach. 
= Arthonia radiata Ach. 
A. spectabilis Ach. 
= Arthothelium  spectabile 
Mass. 
A. punctiformis Ach. 
A. glebosa Tuck. 


C.; Newf. 
& 
CerEiics 


4. Group: COLLEMAE Hill. 


Family 1. Collemaceae 


Collema microphyllum Ach. 
= Leptogium microphyllum 
(Ach.) Zahlbr. 

C. tenax (Sw.) Ach. 

C. furvum Ach. 

C. myriococcum (Ach.) Arn. 

C. pycnocarpum Nyl. 
= Synechoblastus pycnocar- 
pum (Nyl.) Fink. 

C. verruciforme Nyl. 

C. cyrtaspis Tuck. 
= Synechoblastus cyrtaspis 
(Tuck.) Fink. 

C. leptaleum Tuck. 

C. floccidum Ach. 
= Synechoblastus flaccidus 

(Ach.) Trev. 

C. nigrescens (Leers) Wain. 

C. nigrescens leucopepla Tuck. 
=C. vespertilio (Lightf.) 
Wain. 

C. ryssoleum Tuck. 
= Synechoblastus ryssoleus 
(Tuck.) Fink. 

C. pulposum (Bernh.) Ny]. 


CC 

(or 

Cc: 

C.; Limestone, N. Y. 
(CePA: 

(Cos 1Pal 

(C. 

(oe 


@3;) Jas ValaSet 


CG: 
Bats. to N. J. 
Cee ale 


CxpPale 


ce sage 


ez 


Genus 2. 


Genus 3. 
Genus 4. 


Genus I. 


Genus I. 


Genus I. 


Genus 


= 


Genus I. 
Genus 2. 
Genus 3. 


93 


C. plicatile Schaer. 
= Leptogium plicatile (Ach.) 
Nyl. 

Leptogium bolacinum Stizenb. 
= Dentriscocaulon bolacinum 
Nyl. 

L. tremelloides (L. fil.) Wain. 

L. myccochorum saturinun 

Schaer. 

. palmatum (Huds.) Mont. 

. chloromelum (Sm.) Nyl. 

. dactyinum Tuck. 


SUIS ist le 


. lacerum (Sm.) Fr. 

= L. scotinum (Ach.) Fr. 
L. pulchellum (Ach.) Ny]. 
L. saturinum (Dicks.) Ny. 
L. tenuissimum (Sm.) Koerb. 
Synechoblastus (see Collema). 
Dendriscocaulon (see Lepto- 
gium). 


Ulster Co., N. Y. 


C7 y Bian Catecaa: 


(Oe 

Cc 

Pale 

Pal.; Poughkeepsie, N. Y. 
Gea 


C- 
(Ce 
€ 


Family 2. Heppiaceae 


Heppia Despreauxii (Mont.) 
Tuck. = H. virescens 
(Despr.) Nyl. 


Cam. 


Family 3. Lichinaceae 


Lichina confinis Ag. 


Pal. 


Family 4. Pyrenopsidaceae 


Pyrenopsis Schroederi (Mass.) 
Nyl. 
= Psorotichia Schaereri 
(Mass.) Arn. 


Sus. 


Family 5. Ephebaceae 


Ephebe pubescens Fr. 
= FE. lanata (L.) Wain. 


CheeSuss 


Sub-order: CONIOCARPINEAE Meyer, 


Family 1. Caliciaceae 


Chaenotheca (see Calicium). 
Stenocybe (see Calicium). 
Calicium tigillare (Fee) DC. 
= Cyphelium tigillare Th. 
Fr. 
C. byssacaum Fr. 
= Stenocybe byssacaum 
(Fr.) Nyl. 


CepAt: 


Genus I. 


Genus I. 


Genus I. 


*Genus 2. 


*Genus 3. 


*Genus 4. 


*Genus I. 


94 


C. Curtisii Tuck. 

C. curtum Turn. & Borr. 

C. fuscipes Tuck. 

C. phaeocephalum (Turn.) 
Turn and Borr. & 
= Chaenotheca phaeoceph- 
ala (Turn.) Th. Fr. 


A090 


C. roscidum roscidilum Ny]. (ee 
C. roscidum (F1.) Nyl. Ocean, N. J. 
C. subtile Fr. Cc. 
= C. parieturnum Ach. 
C. tubaeforme Tuck. c: 


II: Order PYRENOCARPALES Wain 


Family 1. Mycoporaceae 
Mycoporum pycnocarpumNyl. C. 


Family 2. Trypetheliaceae 


Try pethelium virens Tuck. @: Pali: Ogden; Pa: 


T. cruentium Mont. Salem, N. J. 
= Milanotheca cruenta 
(Mont.) Miill. Arg. 


Family 3. Pyrenulaceae 


Pyrenula hylaspora (Nyl.) 


Tuck. (C5 
P. lactea (Mass.) Tuck. CG: 
P. thelaena (Ach.) Tuck. CG: 
P. pachycheila Tuck. Newf. 
P. nitida (Weig.) Ach. CeiGCat: 


or P. nitida (Schrad.) Ach. 
P. punctiformis (Ach.) Naeg. C.; Cat. 
P. cinchonae Tuck. Newf. 
P. leucoplaca (Walbr.) Koerb. C. 
Lepthorapsis derinidis (Ach.) 


The Er: Ce PalieAt 


= Sagedia oxespora (Nyl.) 
Tuck. 
Porina faginea (Korb.) Arn. Cc: 
= Sagedia lactea (Korb.). 
Polyblastiopsis lactea (Korb.) 
Zahlbr. C 
= Sagedia lactea (Kbr.) 


Family 4. Dermatocarpaceae 


Dermatocar pon arboreus (Fr.) 
Fink. C.; Newf. 
= Endocarpon arboreum 


jolt 


- W. 


d. w. 
d. w. 


ig 


d. w. 


(Schweinitz). 
D. hepaticum (Ach.). 3-7 Pale d. w. 
= FE. hepaticum Ach. 
D. rufescens (Ach.) Zahlbr. (er d. w. 
= FE. rufescens (Ach.). 
D. miniatum (L.) Mann. Oranges Cow Ne, Ye: 
= E. miniatum (L.) Schaer. Youngs, L. I. d. w. 
D. fluviatile (Weis.) Th. Fr. (ox t. 
= FE. miniatum aquatium 
Schaer. 
D. miniatum complicatum Sw. C.; Pal. t. 


= E. miniatum complicatum 
Schaer. 
Family 5. Verrucariaceae 


Genus 1. Thrombium (see Verrucaria). 

Genus 2. Verrucaria epigaea (Pers.) 
Ach. c: t. 
=Thrombium epigaea(Pers.) 
Walbr. 

V. nitida Schrad. (Ce ie 
= Pyrenula nitida ‘Ach.) 
Weig. 
’ Boys Hicu ScHoot, 
BROOKLYN, N. Y. 


NEWS ITEMS. 


Dr. M. A. Brannon, dean of the college of letters and science, 
and professor of botany, at the University of North Dakota, 
assumed the duties of president at the University of Idaho on 
April 1. 

Professor Bohumil Shimek, of the department of botany, 
University of Iowa, sailed for Europe on April 9. He will spend 
six months abroad studying the work and methods of various 
European universities, and will devote considerable time to a 
study of the loess formations of the Old World. Professor Shimek 
will deliver a series of lectures at the University of Prague during 
May and June. . 


We !earn from Science that the seventieth birthday, on March 
25, of Professor Adolf Engler, the director of the Royal Botanic 
Garden and Museum at Dahlem, near Berlin, was celebrated in 
the presence of many eminent German and foreign botanists, 
by several functions. According to the account in Nature, on 


96 


the day itself, Professor Pax, rector of the University of Breslau, 
with Professors Diels and Gilg, as its editors, presented to Pro- 
fessor Engler a copy of the Fest-Band of Engler’s “Botanische 
Jahrbiicher.”” The volume forms a supplement to the fiftieth 
volume of this publication, and consists of more than forty 
illustrated contributions, largely from his pupils. Professor 
Haberlandt presented Professor Engler, on behalf of hundreds of 
subscribers, with his life-size marble bust, the work of the 
sculptor, A. Manthe. On March 26 there was a banquet at 
which the official world was represented; and on March 27 the 
monthly meeting of the Deutsche Botanische Gesellschaft was 
converted into an ‘“‘Engler’’ meeting, and Professor von Wett- 
stein gave, by special invitation, a lecture on the phylogenetic 
evolution of the Angiosperm flower. 


Mr. G. R. Bisby of the staff of the Brooklyn Botanic Garden, 
has been given a leave of absence from the garden, in order to 
accept a position as plant pathologist for the season with a potato 
grower of northern Maine. He is working under general super- 
vision of Dr. Melhus of the U. S. Department of Agriculture. 


‘The Austrian Zoological and Botanical Society has awarded 
the Archduke Rainer gold medals to two members of Yale 
University, Dr. Ross G. Harrison, Bronson professor of com- 
parative anatomy, and Dr. George R. Wieland, lecturer in 
paleobotany. 


We learn from the daily papers of the death on April 28, at Paris, 
of the botanist Philippe Edouard Leon Van Tieghem. He was 
born on the roth of April, 1829, at Bailleul, France. He was an 
officer of the Legion of Honor, was perpetual secretary of the 
Academy of Sciences, Paris, and was a professor at the Museum 
of Natural History and the Institut Agronomique. He was the 
author of many botanical books and papers, but his most dis- 
tinguished work in recent vears was the editorship of the botanical 
section of the Annales des Sciences Naturelles. 


ie 

The Torrey Botanical Club 
Contributors of accepted articles and reviews who wish six 
~ gratuitous copies of the number of TorREYA in which their papers 
appear, will kindly notify the editor when returning proof. - 

ae Reprints should be ordered, when galley proof is returned 
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#; The following Committees have been appointed for 1914 


Finance Committee Field Committee 
J. H. Barnwart, Chairinan SERENO STETSON, Chairman 
Miss €;-C. Haynes -— 


Budget Committee Program. Committee 
J. H. Barnuart, Chairman Mrs. E. G. Britton, Chairman 
N. Le Britton Miss JEAN BROADHURST 
B. O. DopGE C. SruaRt. GAGER 
M. A. Howe rey SEAVER 
AL W. Evans 
H. H. Russy 


Local Flora Committee 
- N. L. Britton, Chairman 


- Phanerogams: ’ Cryptogams: 
FE. P. BicKNELL ~ as Mrs. E. G. Britton 
N. L. Brrrron —. PHitie DowELy 
eden CH CURTIS! «. Shee Tracy E. Hazen 
-K) Ki Mackenzie > | M. A. Howe 
Norman Tayror : W. A. Morrie 


_ Delegate to the Council of the New York Academy of Sciences 
Wiruiam MansFIELp 


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ORREYA _ 


A Montuty Journat or Boranicat Notes anp News 


EDITED FOR 
THE TORREY BOTANICAL CLUB 
BY 
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JOHN TORREY, 1796-1873 
CONTENTS ~ 
Some Midwinter Algae of Long Island Sound: M. A. HOWE.....-+.000csecercesse ceees OF 

_ Occurrence of the Indian Pipe in a Xerophytic Habitat: E. D. HuLL...-:...... ena b cep 
Two new Tertiary Species of Trapa : E. W. BERRY... ccs1ccccceccecceceseoeeceeseneeeeaaes 105 

Shorter Notes” ink ral om ! 
_. Whorled leaves in Gentiana: E, J. HILl......-.-..2..-csee een: eres aren OP 108 
Se RPROVIEWS ANG NOLES) 65.267 icce cose sins gavcienincn ecawtgses ther ecu sonts cose nen ssnehe Seiezelns otenbiness 109 
BeBe HIN soi P se ae NC Ress eRe oe roo ecg de do enercaazeteda de 112 


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THE TORREY BOTANICAL CLUB 


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+ Columbia University, New York City 


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NORMAN TAYLOR 


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TORREYA 


June, 1914. 
Vol. 14 No. 6 


SOME MIDWINTER ALGAE OF LONG ISLAND SOUND 


By MARSHALL A. HOWE 


For reasons that are more or less obvious the marine algae of 
the coasts of New York and New England have received little 
attention from collectors during the coldest months of the year. 
Mr. F. S. Collins once published in Rhodora* a brief paper on 
“Seaweeds in Winter ’”’, with a specific allusion to his experiences 
“at a point on the shore of Long Island Sound”’ on an intensely 
cold first day of January. Professor Bradley Moore Davis has 
more recently in his important contributions to the “ Biological 
Survey of the Waters of Woods Hole and Vicinity ”’ (p. 474) given 
a list of fifty-four species of algae ‘“‘known to be present in the 
cold-water sublittoral formation of the winter and spring’”’ and 
he remarks that the water temperatures for this formation prob- 
ably average under 35° F. for at least two and a half months. 
Exact dates are not given, but it seems to be implied that any 
one of the fifty-four may be found during the coldest weeks of 
the year. A chart illustrating the algal flora of Spindle Rocks at 
Woods Hole on December 30, 1904, includes eighteen species and 
another for March 17, 1905, shows ten species. In the detailed 
list of the species of the Woods Hole region there are remarks on 
the seasonal distribution of each, such as ‘ 
undoubtedly at other seasons,” ‘‘summer, undoubtedly through- 
out the year,’ ‘“‘at all seasons,’ etc. In a recent interesting 
papert on “The Seasonal | ife-Cycle of some Red Algae at Woods 
Hole”’ Professor I. F. Lewis outlines the life-history of several 


99 66 


“summer, summer, 


* 2: 130-132. 1900. 
7 Plant World 17: 31-35. I914. 
[No. 5, Vol. 14, of TORREYA, comprising pp. 73-96, was issued 14 May 1914.| 


97 


LIBR 4 
NEW y 
BOT ANT 
GARDI 


98 


common red seaweeds of that region, but makes no specific. 
references to midwinter observations. 

The present notes have been suggested by several small collec- 
tions of marine algae made at and near Orient, New York, by 
Mr. Roy Latham during the month of February of the present 
year, a February, by the way, that ranks among the coldest 
ever recorded by the New York City station of the United 
States Weather Bureau. Most of the specimens were found 
washed ashore after heavy storms and may have been passing 
the winter in the deeper waters, but there seems to be nothing 
in the list to excite suspicions as to the actual local occurrence 
of the species found. 

The four following species were found ‘‘near the shore of 
Gardiner’s Bay”’ on February 7: 

Scytosiphon lomentarius (Lyngb.) J. Ag. Plants 14-20 cm. 
long with well-developed gametangia. 

Cystoclonium purpurascens (Huds.) Kiitz. Plant (or frag- 
ment) about Io cm. high and incipiently tetrasporic. Cysto- 
clonium is annotated by Davis as a summer plant at Woods Hole. 

Agardhiella tenera (Ag.) J. Ag. A battered and weather-worn 
fragment with immature or somewhat abnormally developed 
tetrasporangia. Occurring with undoubted Cystoclonium pur- 
purascens, the specimen might possibly be suspected of represent- 
ing a coarse denuded condition of that species, but the mode 
of branching and the larger cells of the inner cortex as well as 
the stouter habit indicate that it belongs with A gardhiella tenera. 
Lewis considers this a summer species at Woods Hole, but Davis 
remarks of it, ““summer, undoubtedly at other seasons.” 

Ceramium rubrum (Huds.) Ag. Apparently sterile. 

The species of the list immediately following were found on the 
shores of the Sound on February 14, just after a severe storm: 

Ulva Lactuca L. 

Desmarestia aculeata (L.) Lamour. The denuded autumn and 
winter condition. 

Laminaria A gardhu Kjellm. 

Laminaria digitata (L.) Lamour. 

Chondrus crispus (L.) Stackh. Tetrasporic. 


99 


Gymnogongrus Torreyi (Ag.) J. Ag. This is probably only a 
peculiar flattened condition of Ahnfeltia plicata, as has been 
pointed out by Professor Setchell.* The flattening, however, as 
in Agardh’s type specimens, is often pronounced in the upper 
parts of the plant, the longer transverse axis being sometimes 
twice as long as the shorter. 

Ahnfeltia plicata (Huds.) Fr. } 

Sterrocolax decipiens Schmitz. Abundant on “Gymnogongrus 
Torreyi,’ which fact may be interpreted as strengthening the 
idea that G. Torrey is only a form of Ahnfeltia plicata. 

Cystoclonium purpurascens (Huds.) Kiitz. Apparently sterile. 

Rhodymenia palmata (L.) Grev. Large tetrasporic specimens 
attached to Laminaria stalks. 

Polysiphonia elongata (Huds.) Harv. Apparently sterile. The 
specimens are in part fibrillose and in part represent the coarse 
denuded autumn and winter condition. Davis ascribes the 
species to “‘summer,”’ but Farlow? recognizes its perennial habit. 

Spermothamnium Turnert (Mert.) Aresch. Attached to the 
base of Polysiphonia elongata. 

Callithamnion Baileyi Harv. With mature cystocarps. 

The following were collected on February 25. Mr. Latham 
writes that the Chaetomorpha, the Sargassum, and the Champia 
were taken by cutting a hole “‘through fifteen inches of ice on 
the bay”’: 

Chaetomorpha Linum (Miill.) Kiitz.t 

Sphacelaria cirrhosa (Roth) Ag. Attached to Ascophyllum (?) 
and forming tufts 0.5-1.5 cm. high. Davis refers this to the 
summer species. 

Desmarestia aculeata (L.) Lamour. 

Sargassum Filipendula (Ag.) J. Ag. A plant nearly 5 dm. high, 

* Rhodora 7: 136-138. 1905. 

7 Mar. Alg. N. E. 172. 1881. 

i Ch. Linum has been referred to Ch. aervea (Dillw.) Kiitz. as a form by F. S. 
Collins (Green Alg. N. Am. 325. 1909). The plant described by Dillwyn may 
be the natural type of the species, but that described by Miiller more than thirty 
years earlier would appear to be the historical type, and, if one is to be considered 
a form of the other, the rules of botanical nomenclature as now almost universally 


interpreted and applied would seem to demand that Mr. Collins’ procedure should 
be reversed and that Ch. aerea should be regarded a form of Ch. Linum. 


100 


somewhat darkened and with scarcely developed receptacles, 
but otherwise of about the normal habit. 

Phyllophora membranifolia (Good. & Woodw.) J. Ag. Tetra- 
sporic. 

Champia parvula (Ag.) Harv. Plants 3-4 cm. high, apparently 
sterile. This species is ascribed to summer by Davis. 

Delesseria sinuosa (Good. & Woodw.) Lamour. A battered 
tetrasporic plant. 

Polysiphonia elongata (Huds.) Harv. Plants 10-15 cm. long, 
fibrillose, apparently sterile. 

Melobesia Lejolisit Rosan. On leaves of Zostera. 

Dermatolithon pustulatum (Lamour.) Fosl. Onleaves of Zostera, 
with the preceding. 

Mr. Latham sent in for determination several collections also 
that were made in the month of March and so are perhaps not 
properly to be referred to as ‘‘midwinter”’ algae, but two of these 
collections were so little later than the month of February that 
they are of some interest in this connection. The first of these 
March specimens were picked up on the “Sound shore’’ on 
March 5, but are believed to have washed in “with the great 
storm of March 1.’’ Omitting the common Fucaceae and a few 
others already mentioned, those of March 5 were 

Halothrix lumbricalis (Kiitz.) Reinke. On Zostera leaf, fertile. 

Punctaria latifolia Grev. Sterile. 

Desmarestia viridis (Mill.) Lamour. 

Chondrus crispus (L.) Stackh. Tetrasporic and cystocarpic. 

Phyllophora membranifolia (Good. & Woodw.) J. Ag. Tetra- 
sporic and cystocarpic plants. The ‘“‘nemathecia”’ of this 
species are in structure very suggestive of Actinococcus sub- 
cutaneus (Lyngb.) Roseny., parasitic on Phyllophora Brodiaet. 
In form, however, they are strikingly different from the sub- 
spherical thalli of Actinococcus subcutaneus and a microscopical 
examination seems to indicate that they are integral parts of the 
Phyllophora thallus rather than parasitic organisms. The re- 
cently established facts as to alternation of generations in the 
Florideae, together with the obvious structural resemblances 
just alluded to, suggest a further consideration of Reinke’s idea* 


* In Darbishire, On Actinococcus and Phyllophora. Ann. Bot. 13: 264. 1890. 


101 


that Actinococcus subcutaneus may really be ‘“‘an asexual genera- 
tion of Phyllophora Brodiaet, growing parasitically on the sexual 
generation.” Darbishire (Joc. cit.) succeeded in showing that 
the thallus of Actinococcus subcutaneus develops from a spore 
that enters the thallus of the male plant of Phyllophora Brodiaei 
through an antheridial ostiole, but he was not able to discover 
whence the spore came or whether it was a tetraspore or a carpo- 
spore. 

Polysiphonia urceolata formosa (Suhr) J. Ag. Sterile. 

Rhodomela subfusca (Woodw.) Ag. Tetrasporic. 

Ceramium rubrum (Huds.) Ag. Tetrasporic. 

Rhododermis Georgii (Batt.) Collins. Forming cushions on the 
margins of Zostera leaves, with pinomsaett: 

Corallina officinalis L. 

On March 7, Pylaiella littoralis (L.) Kjellm., Polysiphonia 
nigrescens (Dillw.) Grev., and Epilithon membranaceum (Esp.) 
Heyd. were added to the foregoing lists. 


NEw YorK BOTANICAL GARDEN. 


OCCURRENCE OF THE INDIAN PIPE (MONOTROPA 
UNIFLORA) IN A XEROPHYTIC HABITAT 


By EpwIN D. HULL 


The Indian pipe (Monotropa unzflora) is considered one of the 
most mesophytic of our plants, and the habitat in which it grows: 
is supposed to conform to its nature. The 7th edition of Gray’s 
Manual gives the habitat of this species as, ‘“‘Rich and dark 
woods.” S. Coulter (1) says, “Indicative of rich soil.” I have, 
however, found it growing sparingly on the oak dunes about 
Lake Michigan at Miller, Lake Co., Indiana, where it seems to 
be the only mesophyte in an otherwise distinctly xerophytic 
flora, at least so far as the vascular plants are concerned. The 
trees of this association, of which the black oak (Quercus velutina) 
far exceeds all the other species in abundance, stand some dis- 
tance apart and permit considerable light to penetrate, so that 
the forest is decidedly open rather than dark. The undergrowth 
does not form a continuous mat, and there are numerous broad 


102 


patches of barrensand. Cowles (2) in 1899 described the ecology 
of these dunes, and showed conclusively that the flora is xero- 
phytic. Coulter (1) listed the vascular plants of these oak dunes, 
totalling 43 species, all of which are of a xerophytic character. 
The nature of the situation is best shown by listing some of the 
most conspicuous and abundant plants contributing to the 
undergrowth. These are Pieris aquilina, Lupinus perennis, 
Viola pedata lineariloba, Opuntia Rafinesqui, Vaccinium penn- 
sylwanicum and Phlox pilosa. The Indian pipe, not being 
abundant, seems to have been entirely overlooked by the numer- 
ous investigators of the sand dune flora. Its scarcity, however, 
may be due to other than edaphic causes. Coulter (1) reports 
it as widely distributed throughout Indiana, but not abundant, 
so it may be as common here as in more mesophytic areas in the 
state. This author listed the counties in which the plant has 
been found, but it seems not to have been reported from any of 
the counties bordering the lake, nor from any of the counties 
adjacent to these, although it doubtless occurs in all. I 
found at the above mentioned station September 15, 1912 a 
single clump of this species at the base of a black oak (Quercus 
velutina), consisting of three stalks, evidently of recent appear- 
ance, as the summit of the stems showed no tendency to become 
erect as is the case when the fruit matures. Stalks of the pre- 
ceding year were also found. Early in October of the same year 
I found in a similar situation at Dune Park, a few miles east of 
Miller, another clump of these plants with the seeds nearly all 
shed. It is seen, therefore, that the aerial life of this species 
is very brief, doubtless of less than a month in duration, at least 
in this locality. While the plants found at Miller were some- 
what dwarfed, the two dried stems before me measuring II and 
12.5 cm., they are considerably above the minimum height, .5 
dm., given in Gray’s Manual. 

It should be here noted that Coulter (1) reports tke species 
as occasional on dry wooded hillsides in the southern counties of 
Indiana, and I have myself found it on the summits of dry oak 
covered hills in DeWitt Co., Illinois, where the plants are locally 
abundant. Such habitats, while probably not nearly so xero- 


103 


phytic as the oak dunes of Lake Michigan, are not of an extreme 
mesophytic character by any means. I have noticed that in 
these Illinois plants the culmination of the flowering period is not 
reached until the latter part of August or early September, but 
the flowers do not come so late as in plants of the sand dunes. 
That the habitat, in DeWitt Co., at least, is more mesophytic, 
is indicated by the distribution of the xerophytic fern (Pteris 
aquilina) in that county. Herein the dunes this fern is associated 
with the oaks, but in the oak woods of DeWitt Co. it is entirely 
absent, occurring only on barren, exposed hills, the most xero- 
phytic areas in the region. The situation in southern Indiana 
may be the same. 

The late blooming, September 15, is also noteworthy. Coulter 
(1) gives the blooming period as extending from June to August, 
which is the exact time given in Gray’s Manual. ' It is interesting 
that xerophitism, often so potent a factor in early blooming, 
seems to have a reverse effect on the flowering of this species. 

To account for the occurrence of this mesophyte in a xerophytic 
area, there seems to me two theories which should be considered. 
One theory would be that some local condition, comparable to the 
usual mesophytic habitat of this species, exists. A second view 
would be that the plant is able to endure xerophytic conditions 
on account of its short aerial life, provided there is sufficient 
stable humus to enable the underground portion to persist from 
year to year. An alternative, of course, would be to consider 
the plant as a xerophyte, but there is no evidence to support 
such an assumption. 

Of the two theories the second seems to be the more valid one. 
About the only evidence to support the first view is that appar- 
ently the plants are here subjected to rather severe conditions, 
as is shown by the scarcity and semi-dwarfness of the stems, 
these being also much blackened by the sun. But such evidence 
may be more apparent than real, for the plant is able to persist 
and ripen its seed as well here as elsewhere. To support the 
second view we have the evidence of late blooming, which seems 
to me very important. If a local condition existed, the plant 
would be expected to flower in its usual season. Cowles (2) 


104 


has shown that even in the open shifting sand between the oaks, 
a very xerophytic situation, such fungi as various species of 
Geaster and Lycoperdon occur. Plants like these can hardly be 
called xerophytes, but on the contrary are extremely mesophytic, 
the entire aerial life of the plant being of extremely brief duration. 
Otherwise the plants probably exist only as spores, the delicate 
mycelium being unable to withstand any severe or prolonged 
drought. Of similar habit are many desert plants, both annual 
and perennial, which spring up during wet seasons and persist in 
dry periods only underground, or as seeds. These plants, as 
pointed out by Schimper (3) possess no xerophytic structures, 
and would, therefore, be called mesophytes. Comparable in 
habit to these desert perennials, it seems to me, is the Indian 
pipe, although, unlike them, its activity must be confined to a 
definite period, on account of seasonal changes in temperature. 
The question might naturally be raised that if the plant is able 
to live in xerophytic habitats, it should also be found in the more 
exposed places, as are the fungi. But the peculiar short root 
system of this species would be exposed quickly by a shifting of 
the sand, even though slight, and the plant would necessarily 
perish. As I have stated, the fungi probably exist over severe 
periods in the form of spores, while the Indian pipe cannot pro- 
duce fruit in a single season from the seed, in all probability, so 
that a stable soil is requisite. 

It would seem, however, that the plant is confined to woodland: 
habitats, whether mesophytic or otherwise. Sunlight, as is well- 
known, causes a blackening of the stems, and extreme sunlight 
would doubtless kill them. It is unlikely, therefore, that the 
plants could exist in the open. But given a degree of shade, it 
seems reasonable to suppose that they could exist in some of the 
most xerophytic places. 

The late mid-September blooming, which seems to be the key 
to the persistence of the plant here, could be accounted for in the 
following manner. Fuller (4), who investigated the evaporating 
power of the air in its relation to the vegetation of the sand dunes, 
has shown that commencing about the first of September there is 
a decided drop in the rate of evaporation and this drop continues 


105 


during the greater part of the month, when the rate begins to rise 
on account of the trees shedding their foliage. By the latter 
part of September the rate of evaporation is at its lowest expres- 
sion during the period under observation, namely, from May to 
October, inclusive. This low rate of September forms a striking 
contrast to the high rates of much of June and all of July and 
August, the usual flowering period of this species. It is during 
this period of low evaporation that the stems of the Indian pipe 
spring up, flower and mature their fruit. 

From the above data it would seem that the Indian pipe is a 
‘mesophyte, but so far from being confined to mesophytic woods, 
is able to persist in decidedly xerophytic areas. It seems, how- 
ever, to be confined to woods. This persistence is determined 
by the short aerial life of the plant, and not by the formation of 
any xerophytic structures. 


CHICAGO, ILL. 
LITERATURE CITED 


I. Coulter, S., A Catalogue of the Flowering Plants and the Ferns and their Allies 
Indigenous to Indiana. Indiana Dept. of Geology and Natural Resources. 
24th Annual Report, pp. 553-1002. 1899. Data concerning the Indian 
pipe is given in pp. 867-868. 

2. Cowles, H. C., The Ecological Relations of the Vegetation on the Sand Dunes 
of Lake Michigan. Bot. Gazette 27. 1899. The oak dunes are described 
in pp. 379-382. 

3. Schimper, A. F. W., Plant-geography upon a Physiological Basis, pp. 610-612. 
Oxford, 1903. 

4. Fuller, G. D., Evaporation and Plant Succession on the Sand Dunes of Lake 
Michigan. Transactions Illinois State Academy of Science 4: 119-125. 
IQII. 


VO NE Wore PNR SPE CIbS OF TRAPA 


By Epwarp W. BERRY 


The genus Trapa, formerly included in the family Onograceae, 
is now made the type and only genus of the Hydrocaryaceae 
(Trapaceae, Dumort, 1827). There are three existing species, all 
aquatics, and all confined to the Old World except tor the naturali- 
zation of Trapa natans L., in New England and New York. The 
latter species is found irregularly scattered throughout central 
and southern Europe, its area of distribution being a contracting 


106. 


one as shown by its occurrence in post-glacial deposits at very 
many localities beyond its present range in Russia, Finland, 
Sweden and Denmark. The two other existing species are 
Trapa bicornis L., and Trapa bispinosa Roxb., of southeastern 
and southern Asia and said also to occur in Africa. 

The genus has an extended geological history. Rosettes sup- 
posed to represent the floating leaves (Trapa ? microphylla Lesq., 
and Trapa ? cuneata Knowlt.) are widespread in the Rocky 
Mountain province in beds of late Cretaceous and early Tertiary 
age. The oldest recognizable fruits are a large bi-cornute form 
from the Eocene of Canada and Alaska and Trapa wilcoxensis de- 
scribed in the following paragraph. An Oligocene species (Trapa 
Crednert Schenk) has been described from Saxony, and no less 
than seven species have been described from the Miocene—two 
occurring in Idaho (Payette formation), one in Japan and the 
balance in Europe, where two species continue into the Pliocene. 
A species from the late Pliocene of America is also described in 
the present note. The existing Trapa natans has been recorded 
from the preglacial beds of England and Saxony and from very 
many interglacial and postglacial deposits in Portugal, Italy, 
Netherlands, Germany, Sweden, Russia and Denmark, Gunnar 
Andersson in a recent paper (1910) mentioning 18 localities in 
West Prussia, 6 in Denmark, 17 in Sweden and 29 in Finland. 
With this short prefatory statement the two following species 
may be briefly characterized. 


Trapa wilcoxensis sp. nov. 


Fruit relatively small, rhomboidal in outline, wider than high, 
indehiscent, coriaceous, armed with two more or less extended, 
laterally directed or ascending (not recurved) horns. Width 
1.3 cm. to 1.8 cm. Height 7 mm. to 9 mm. Somewhat com- 
pressed (naturally), expanded medianly, broad and extended 
below, more or less extended and rounded above. Horns stout, 
conical, more or less extended. Surface more or less tuberculate 
medianly. Figs. 1-3. 


This species comes from the middle Wilcox of the Lower 
Eocene at Peryear, Henry County, Tennessee. It shows con- 
siderable variation in size and relative development of horns and 


107 


is not particularly close to any previously described form. While 
much smaller than the existing species it is clearly referable to 
Trapa. Itisacurious fact that nearly all of the North American 
Trapa have two horns like the existing Asiatic species instead 
of four as is normally the case in the existing European species. 


Trapa alabamensis sp. nov. 


Coriaceous nuts, rhomboidal and roughly bilateral in outline, 
much swollen and tuberculated medianly, with normally two, 
short, conical, acuminate, slightly recurved horns. The base is 
rounded and shows a conspicuous scar. The sides are somewhat 
unsymmetrical and faintly and irregularly ribbed and usually 
show three large tubercles on each face above the middle. The 
base is large and full. The apex is but slightly produced or 
truncated. Length from tip to tip of the horns about 4 cm. 
Height about 2cm. Figs. 4, 5. 


Fic. t. Fruits of Tertiary Trapa; 1-3, Trapa wilcoxensis from Lower Eocene of 
Tennessee; 4, 5, Tvapa alabamensis from the Pliocene of Alabama. 


The present species is very close to the existing Trapa natans 
especially to the two horned variants (the species is normally four 
horned). The latter is larger and more symmetrical with 
stouter more recurved horns, and a more extended apex as well 
as a stouter and more symmetrical body. The present species is 
common in the late Pliocene clays of Red Bluff, Perdido Bay, 
Baldwin County, Alabama, and inland from the present Gulf 
coast to elevations of over 300 feet near Lambert, Mobile County, 
Alabama. 


108 


Both o1 these new species are of great interest since they are the 
first recorded indigenous forms from the eastern United States 
and show that the genus was present in this area throughout the 
Tertiary. They alse throw an interesting light on the conditions 
of sedimentation at the time of their existence. 


JouNs HopxKINs UNIVERSITY, 
BALTIMORE, MD. 


SHORTER NOTES 


WHORLED LEAVES IN Gentiana.—In his notes on the flora of 
Copake Falls, N. Y., Sereno Stetson describes and gives an illus- 
tration of an unusual leaf arrangement in Gentiana quinquefolia 
L., where whorls of three are shown instead of the normal 
opposite phyllotaxis in Gentiana. Information is requested 
from those knowing a similar case. There is one in mysherbarium 
of G. Andrewsii Griseb., which I collected by Chautauqua Lake, at 
Mayville, N. Y., September, 1907. One stem among those taken 
has four whorls of three leaves, those of the uppermost nodes 
below the leaves subtending the cluster of flowers at the top. 
The stem was cut off near the root, and was about 4 dm. high, 
2 dm. being occupied by the verticillate leaves. The four lower 
nodes represented on the stem have the leaves opposite, so that 
the entire stem does not share in the abnormality. One leaf 
in the upper whorl has a flower in its axil. The only mention I 
have seen of a similar case, except that of Mr. Stetson, is by Dr. 
O. Penzig in his Pflanzen-Teratologie (2: 155. 1894). Under 
Gentiana asclepiadea L., a plant of southern Europe, he says: 
‘“‘Whorls of leaves with three members in place of the pair, not 
rare.” 


Dalia JalMicit,. 


CHICAGO, ILL. 


109 


REVIEWS 


Gibson’s Supplement to Jost’s Piant Physiclogy* 


This is an unusual type of book, and difficult to review. 
Botanists are familiar with Gibson’s English translation of the 
first German edition of Jost’s work. A second German edition 
contains so much new matter, and other extensive alterations as 
really to call for a new English translation. Scientific books of 
971 pages, however, are expensive, and of doubtful financial 
success, especially when a second edition follows a first within 
a very short time, and this fact, quite probably, is the explanation 
of this supplement. 

It aims to give all the changes in the second edition as com- 
pared with the first. Herein, the reviewer believes, lies its 
weakness, for much that is unimportant, or not essential, is 
necessarily included, and this becomes irritating and wasteful 
of one’s time. For example, of what vital importance is it that 
on page 199, line 41, of the first edition, one should read ‘‘leading 
even to’’ vs. “‘leading to” (Supp. p. 58); or on page 202, line 55, 
“If glucose,” vs. “When glucose’”’ (Supp. p. 59); or that on p. 
205, Il. 55-56, ““many unending’’ should be read ‘‘an endless 
number of’’ (Supp. p. 63); or that on page 405, Lecture XXXII 
is XX XI in the second German edition (Supp. p. 128), et cetera, 
throughout the Supplement? 

In short, it seems to the reviewer that it would have been 
preferable to have included in the Supplement only the new 
matter of the second German edition, and important errata. It 
is for the new matter that the Supplement will undoubtedly be 
valued and consulted, the numerous summaries of recent work, 
or new summaries and references to older work being especially 
welcome. These are found in connection with the topics of © 
photosynthesis, protein synthesis, respiration, fermentation, and 
elsewhere. Many, if not most, students of experimental evolu- 
tion will no doubt be surprised as well as interested to read (on 

* Plant Physiology, by Dr. Ludwig Jost. Authorized English Translation, 
by R. J. Harvey Gibson. Supplement, Incorporating the Alterations of the 


Second Edition of the German Original. Pp. 1-168. Oxford, at the Clarendon 
Press, 1913. Price, 2s. 6d. net. 


110 


page 125 of the Supplement) Hofmeister’s clear statement made 
in 1868, to the effect that mutation, rather than continuous 
variation, supplies the material for selection in species making. 
“New forms,” said Hofmeister, ‘‘do not come into existence by 
the summation in successive generations of small differences from 
the customary form, all tending in the same direction; they 
appear suddenly, and are widely different from the parent.” 

If America were as Teutonic in the matter of the publication 
of scientific books, as it is in the organization of education, 
and of scientific research, we would not have to rest content with 
supplements, but would early enjoy an American translation of 
the second German editions of works important enough to run 
into a second edition. C. STUART GAGER. 


Schaffner’s Field Manual of Trees* 


As a field manual to slip in one’s pocket, the present volume 
will unquestionably fill a long felt want, as it condenses the 
information contained in more complete works. The book is 
scarcely more than one quarter inch thick, and only 634 x 4% 
inches long and wide. Brief descriptions are given for the genera 
and species, but not for the tamilies. Keys are provided , 
throughout and the latter feature has been very thoroughly 
covered. ‘“‘Key to the genera of trees in the summer condition,”’ 
“Key to the genera of trees in winter condition,” ‘‘General key © 
to the families and genera,’”’ and ‘‘Key to the fruits” will give 
some idea of the scope and usefulness of this side of the book. 
In the appendix is a “‘General classification of the wood of trees 
included in the manual”’ and a glossary of terms. The classifica- 
tion of woods is based on their structure, porusness, and other 
structural characters. 

Of course the main body of the work is taken up with the 
description of the individual species. All the usual features are 
covered, tersely and concisely, and for practical field work, these 
descriptions will be found quite adequate. There are notes on 

* Schaffner, J. H. Field Manual of Trees, including southern Canada and the 
northern United States to the southern boundary of Virginia, Kentucky, and 


Missouri, westward to the limits of the prairie. Pp. 1-154. R. G. Adams Co., 
Columbus, Ohio. Price, limp cloth, $1.25; limp leather, $1.75. 1914. 


rl 


the uses of the different species, and the geographical distribution 
is given for each kind. 

The nomenclature used is that of the second edigen of Britton 
and Brown's “Illustrated Flora,’’ but the sequence of families is 
that adopted in the work of Clements, Rosendahl and Butters in 
their “‘Minnesota Trees and Shrubs,’ published in 1912. This 
is the ““Besseyan System’’ which differs from the Engler and 
Prantl sequence in following the gymnosperms by the orders 
Ranales, Geraniales, Malvales, Rosales, Celastrales and so on. 
One criticism that can be justly levelled at a purely popular 
hand-book such as this are the names Cassiatae, Fabatae and the 
like, which are categories readily understandable by the trained 
botanist, but will be unfamiliar to the greater part of the readers 
to whom the book is addressed. 

As a workable pocket manual of trees, the book is sure to 
have a wide range of usefulness. Nx. T. 

Warner, C. H., Formaldehyde as an Oxidation Product of 
Chlorophyll Extracts, Proc. Roy. Soc. B. 87: 378-385, 1914, 
reports a series of interesting experiments demonstrating the 
production of an aldehyde when light acts on a film of chlorophyll 
(prepared by allowing an alcoholic or ethereal chlorophyll 
extract to evaporate on glass plates). The production of alde- 
hyde goes on parallel with a bleaching of the chlorophyll, is 
dependent on the presence of oxygen, but independent of the 
presence of carbon dioxide. Along with the aldehyde a volatile 
substance, capable of liberating iodin from a potassium iodide 
solution, is produced. 

In the same number of the Proceedings, Wager, H., The Action 
of Light on Chlorophyll, Proc. Roy. Soc. B. 87: 386-407, describes 
a more varied series of experiments covering essentially the same 
ground. Warner is inclined to consider hydrogen peroxide the 
active oxidizing agent, produced in the presence of oxygen and 
light, which attacks the chlorophyll; Wager argues that probably 
some other peroxide is concerned. 

This work again shows that the original experiments with 
chlorophyll films as performed by Usher and Priestley did not 


112 


demonstrate, as these authors had concluded, the synthesis of 
carbon dioxide and water. 

Warner and Wager both cautiously raise the question whether 
in green leaves a photo-decomposition of chlorophyll gives rise 
to formaldehyde which is then polymerized into sugars, instead 
of there being a direct synthesis of carbon dioxide and water into 
formaldehyde. 

It is to be noted that a number of the experiments described 
seem suitable as laboratory exercises and lecture demonstrations. 


W. G. M. 


NEWS ITEMS. 


The Board of Managers and the Women’s Auxiliary of the 
New York Botanical Garden held a reception and spring inspec- 
tion of the grounds, buildings and collections on the afternoon 
of Thursday, May 7, from three until six o'clock. Tea was 
served in the museum building at 5.20 P.M. About 250 guests 
motored through the grounds and speeches were made by Dr. 
W. Gilman Thompson, one of the committee of the board of 
managers, and by the director, Dr. N. L. Britton. 

“After a lapse of over twenty-one years a botanic garden at 
the Cape is once again an established fact. It is described by the 
Kew Bulletin as ‘thoroughly worthy of a United South Africa.’ 
The choice of the Kirstenbosch estate as the site for the National 
Botanic Garden was a particularly happy one, and there can be 
no doubt that the selection of this site for the purpose would 
have met with the approval of Cecil Rhodes himself. The 
existence of so suitable a site for the garden as is this portion of 
the Rhodes estate would, however, have been of little value but 
for the farsightedness of General Botha and his government, in 
consequence of which the scheme has passed from the region of 
proposition and discussion into the realm of fact. The control 
of the garden is to be exercised by a board of five trustees, of 
whom three are nominated by the Government, one by the Cor- 
poration of Capetown, and one by the Botanical Society. The 


115 


site granted for the garden is a farm about 400 acres in extent on 
the eastern slopes of Table Mountain, which has been neglected 
for some years. Though it is largely overgrown with poplars 
and pines, there still exist on it specimens of nearly every native 
tree to be found in Southern Cape Colony, west of the Knysna 
forests. The general situation of the garden is all that could be 
desired. A feature of very great importance is the presence of 
permanent water, and there are two constant streams, which 
will be of the utmost value for irrigation purposes, and will, no 
doubt, also be capable of effective treatment from the scenic 
point of view, especially as the gorges are richly wooded with 
native vegetation. There is also a heavy winter rainfall, and 
the garden is practically completely sheltered from the drying 
southeast wind.” 


Mr. W. W. Eggleston left New York May 8 for a trip, during 
May and June, to the Manti, Fillmore and Fish Lake Forests, 
Utah and the Kaibab Forest, northern Arizona. This latter 
region, north of the Grand Canon, Arizona, is very little known 
botanically, having been visited by Mr. Ivar Tidestrom in Igog, 
but perhaps not previously, by botanists. 


Dr. N. L. Britton and Mr. Stewardson Brown left New York 
on May 20 for Bermuda where they will study the vegetation, 
returning about June 8. 


Dr. H. A. Gleason, of the University of Michigan, has returned 
from a trip around the world begun last September. He will 
teach the coming summer at the biological laboratory of the 
University of Michigan. Dr. Gleason expects to spend the 
month of September at the New York Botanical Garden studying 
the genus Vernonia. 


It will be a source of regret to local botanists to hear that within 
a short time there will be practically no natural vegetation left 
on the Hempstead Plains. A corporation is now ploughing up 
the virgin prairie with traction machinery and only that part of 
the plains south of the Motor Parkway remains in its original 
state. The corporation intends to plough all the plains as rapidly 
as possible, leasing the ploughed land for agricultural purposes. 


114 


On the afternoon of May 23, a conference was held at the 
Brooklyn Botanic Garden between the garden staff and some high 
school teachers of biology of Greater New York, as represented 
by the New York Association of Biology Teachers. The 
purpose: of the conference was to offer an opportunity for the 
members of the association to become better acquainted with 
the aims, equipment, and work of the garden, and to enable the 
latter to secure from the teachers practical suggestions as to how 
the garden may render the largest service to the teaching of 
botany in New York City and vicinity. Following the conference 
there was an inspection of the first section of the laboratory 
building and the first two sections of the conservatories. The 
second section of the conservatories devoted to tropical economic 
plants, was opened to visitors for the first time on this occasion, 
and will hereafter be open to the public daily. 


a 


- The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six 
sratuitous copies of the number of TorrEyAin which their papers 
appear, will kindly notify the editor when returning proof. | 

~ Reprints should be ordered, when galley proof is returned 
to the editor. The New Era Printing Co., 41 North Queen 
Street, Lancaster, Pa., have furnished-the following rates : 


5 2pp 4pp 8pp 12pp 16pp 20pp 
25 copies $.75 $1.05 $1.30 $1.80 $2.20 $2.50 
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Covers: 25 for 75 cents, additional covers 1 cent each. 
Plates for reprints, 40 cents each per 100. 


The following Committees have been appointed for 1914 


Finance Committee Field Committee 

J. H. Barnuart, Chairman SERENO STETSON, Chairman 
Miss C. C. Haynes 

| Budget Committee Program Committee 
J. H. Barnuart, Chairman Mrs. E. G, Britton, Chairman 
N. L. Brirron Miss JEAN BROADHURST 
B. O. DopGE C. STUART GAGER 
M. A. Howe F, J. SEAVER 
A. W. Evans 7 
H. H. Russy 


Local Flora Committee 
N. L. Britton, Chairman 


Phanerogams: : Cryptogams: 

E. P. BIcKNELL Mrs. E. G. Britton 
N. L. Britton Puitie DOWELL 
Gy Curtis Tracy E. Hazen 

K. K. Mackenzie M. A: Howe 
Norman TAyLor W. A. Murrity 


Delegate to the Council of the New York Academy of Sciences 
WILLIAM MANSFIELD. 


OTHER PUBLICATIONS 
i OF aes 


(1) BULLETIN 


A facintaly journal devoted to general botany, ectlighed 


1870. Vol. 40 published in 1913, contained 712 pages of text | ; 


and 26 full-page plates. Price $3.00 per annum...’ For Eutope, — 
14 shillings. Dulau & Go., 37. Soho) Square, London,. grey 
agents for England. | 7 Tea 
Of former volumes, only 24—40 can be supplied entire ; cer-- 
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Vols. 24-27 are furnished at the published | price of two. ella mel 
each; Vols. 28-40 three dollars each. | 


Sele copies (30 cents) will be furnished only ies not Bie 


breaking complete volumes. 


(2) MEMOIRS | - 

The Memorrs, established 1880, are published at irregulas 
intervals. Volumes 1-13 are now comipleted ; Nos. 1 and 2 of 
Vol. 14 have been issued, The subscription price is fixed at 
$3.00 per volume in advance. The numbers can also be pur-' ~ 
chased singly. A list of titles of the individual papers: oye of ay 
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(3) The Preliminary Catalogue of Anthophyta and Pters | 
dophyta reported as growing within one hundred alee of New : 
York, 1888. © Price, $1.00: 


Correspondence relating to the above publications should be : 
addressed to ; 
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Vol. 14 : July. 1914 : No. 7 


~TORREYA 


On MonTuty JouRNAL OF Horaicas Notes AND News 


\ 
EDITED FOR 
THE TORREY BOTANICAL CLUB 
Ne : BY 
NORMAN TAYLOR 
JOHN TORREY, 1796-1873 
CONTENTS 
The Influence of lena Seasons on the Growth of Yellow Pine: J. E. Kirx- 
RY ODES eters ocr gana aes eet. ee sak Mos BK Red Stace aid Ie py, sabe k yD soe teat es gas ae 2 Pee cy e Ti5 
A New Southwestern Sedge: K. K, MACKENZIE...) c.ee ee  cteete pees 125 
Shorter Notes 
Tri- and Tetracarpellary Walnuts: F. A. MCDERMOTT ....00 0202.20 y ieee 127 
Revie wsrand Wotes 50, kee Cn hcdia ciel speapas dco ese onagysl oan Se 5 SU eae 128 
Selden’s Everyman’s Garden Every Week : N. e BRETTON: cer ohne Wine wae 128 
Proceedings of the Club ............ Br elt OL ee ARAM Deed A er BRE GP pcr ALE SOC in D2 
Nera tern, 25300005 5 est ey GRO UN yA RCA ARR? Pe 131 


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NORMAN TAYLOR 


TorReEyA is furnished to subscribers in the United States and_ 
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PAs 


TORREYA 


July, 1914. 


Vol. 14 No. 7 


THE INFLUENCE OF PRECEDING SEASONS ON THE 
GROWTH OF YELLOW PINE 


By J. E. Kirkwoop 


Many of the mountains of western Montana have no trees 
on their western and southern slopes, except at altitudes above 
4,000 or 5,000 feet. Some support sparse open stands of yellow 
pine and Douglas fir; in such places the ground cover usually 
consists of grasses and a few shrubs. The barren aspect of these 
slopes is due to the desiccating influence of wind and sun, to the 
full force of which they are exposed throughout the growing 
season. The annual precipitation in the vicinity of Missoula is 
15.84 inches, which represents the mean of over twenty years of 
observation. May and June are the months of heaviest rainfall, 
furnishing 4.43 inches of the abovemean. By thesame reckoning 
July and August together furnish 1.95 inches of the annual 
precipitation, and during these months the soil becomes dry to 
a depth so great that only deeply rooted perennials are able to 
survive, and these with growth suspended, or at least very much 
retarded. 

Situations on such slopes, locally more favorable, are occupied 
by incipient forest growth which increases toward the greater 
altitudes, where, owing to the storage of snow and to other 
factors, conditions are more favorable for the growth of trees. 
In this region the yellow pine and Douglas fir are the species most 
resistent to drouth, encroaching gradually upon the prairie, and 
eventually occupying it fully or giving way to other species of 
forest trees. In the margin of the yellow pine type, where the 
prairie and the forest blend, the conditions for forest growth are 


[No. 6, Vol. 14, of TORREYA, comprising pp. 97-114, was issued 8 June 1914.1] 


115 


NE) 


116 


most severe from the standpoint of moisture requirements as 
compared with other forested areas. Under such circumstances, 
therefore, we should expect to see most clearly expressed the 


F.c.1. Part of the crown of a young pine (Pinus ponderosa), showing the height 
growths of the years 1910 to 1913 inclusive. 


influence of any variation in the moisture supply from time to 
time, and especially from year to year. 
The relation of the water supply to metabolism and assimil- 


ALA 


ative activity is well known. It is equally well known that the 
rate of height and diameter increase is the expression of the 
relative abundance of soil moisture, as well as of other elements 
in the essential conditions of growth and development. It has 
been shown that there is a close relation between the annual 
precipitation and diameter growth in the western yellow pine. 
Douglas,* working on Pinus ponderosa near Flagstaff, Arizona, 
found that for a period of years the relative diameter of each 
season, as revealed by careful stem analyses, corresponded closely 
with the relative abundance of moisture in the several years, as 
shown by the weather records of that locality. The results of 
this investigation further showed that the variability in increment 
was in this instance subject to several factors, such as the relative 
porosity of the subsoil, the unequal distribution of soil moisture 
in different directions from the tree, etc.; in short, that any dif- 
ferential distribution of moisture, either topographically or from 
season to season was expressed in a corresponding variation in 
the size and form of the annual rings. The conclusions in this 
paper seem to be supported by the facts presented, and will 
doubtless apply to other regions as well, where the amount of soil 
moisture varies considerably from year to year during the period 
of more rapid growth. Relative height and diameter increase, 
however, are not always the expression of the conditions in the 
same season in which such increase took place, but sometimes 
indicate the factors prevailing in the preceding year. Bogue,f 
as a conclusion from observations at Stillwater, Okla., states that 
“the month of maximum rainfall is the month of maximum 
growth.” As a result of further studies at Lansing, Mich., he 
finds that the width of the ring is proportionate to the rainfall 
within certain limits, but that excessively heavy or light pre- 
cipitation is evidenced by a corresponding growth of the tree in 
the following year, and rightly attributes the difference to the 
difference in the amount of food material stored in the preceding 
season. 


* Douglass, A. E. Weather cycles in the growth of big trees. Monthly 
Weather Review 37: 225-237, June, 1909. 

7+ Bogue, E. E. Annual rings of tree growth. Monthly Weather Review 33: 
250-251, June, 1905. 


118 


The main growth of trees in height and diameter is accomplished 
during the first few weeks of the growing season. The opening 
of the buds in the spring or early summer is followed by the rapid 
elongation of the shoot of the season, and the early expansion of 
its leaves. There after-growth in length is very much retarded, 
and finally ceases with the formation of the terminal bud, which 
is to be unfolded in the following season. This terminal bud is 
formed long before the summer is over and into it are crowded 
the nutritive substances which supply the food for its early 
expansion the following year. Upon the size and vigor of the 
buds thus formed depends the length of the shoot of the following 
season, other things being equal. Likewise the size and vitality 
of the bud are measures, in the main, of the conditions obtaining 
in the seasons in which they were formed. The greater the 
supply of moisture, up to the optimum degree, the more favorable 
the temperature, sunlight, etc., the greater is the reserve force 
in the buds and consequently the more vigorous are the shoots 
issuing from them. 

It is improbable that the whole growth of the new leader is 
at the expense of the food stored in the bud alone. That from 
other parts also doubtless contributes, but the tendency is to 
crowd the formative materials toward the extremities of the 
main shoot and the branch. In the sharing of these materials 
the main shoot leads and the branches follow in the order of their 
importance. The principal growth, however is undoubtedly at 
the expense of the locally stored materials, the substances stored 
elsewhere having their part to play in the development of the 
tissues in their immediate proximity. 

An examination of the buds reveals the cells of the leaf rudi- 
ments and axis densely crowded with a granular material which 
appears to be proteid, responding to several tests for that sub- 
stance. This is in line with what is known concerning the nature 
of reserve materials in trees. The density of the stored substance 
is greatest in the bud, and much less in the stem outside of the 
bud. 

It is a matter of no difficulty to determine by external markings 
the limits of annual growth on the younger portions of the stem 


119 


and branches of most woody plants. Sometimes it is possible to 
trace the annual growth back through twenty five or thirty years 
by reference to the branching system. Pinus ponderosa is a 
favorable subject for study in this particular. At the top of the 
leader a strong bud is formed toward the conclusion of the growing 
season. Close to the base of this bud are formed several lateral 
ones, the subsequent development of which produces a whorl of 
branches. As other lateral buds are usually lacking along the 
shoot of the season, it follows that each circle of branches marks 
the limit of a season’s upward growth of the main stem. As the 
internodes, or spaces between successive circles of branches, do 
not increase in length after they are first formed, the height 
increment of all the past seasons can be determined, so far as one 
is able to identify the distinct whorls which mark the conclusion 
of each year’s growth. 

That the length of the internode in the western yellow pine 
growing in dry situations is an expression of conditions affecting 
growth, not in the present, so much as in the preceding season, is 
now shown with remarkable clearness by the trees of this region.* 
Some of the facts here set forth were observed on an island in 
Flathead Lake during the summer of I913. Trees were growing 
at altitudes varying from four or five to one hundred feet above 
the level of the lake, and in the more open places among the 
mature trees many younger individuals were present varying 
from four to fifteen feet in height. Of many of these it was 
observed that the internode for 191I was considerably shorter 
than that for 1910. Reflecting upon the fact that the season of 
1910 throughout the whole region was exceptionally dry, and 
that of 1911 much more favorable, the question arose as to the 
apparently contradictory evidence of the internodes. Why 
should the growth be less in a season supposedly more favorable, 
and greater in a season obviously less advantageous? 

It is evident that the growth in length in each season is not 
directly affected in this region by the lack of rain in July and 
August, since the elongation of the shoot is practically ended 
before the dry season sets in and before the moisture from winter 


* Pfeffer, W. Plant Physiology, Vol. I, p. 603. 


120 


snows and spring rains disappears from the soil, but indirectly 
by the drouth in the months indicated, as affecting the supply of 
reserve food in the buds and other parts. The supply of food 
stands in direct ratio to the condition of several factors, among 
which the amount of available moisture is very influential, during 
the middle and later summer of the season next preceding. As 
a lack of moisture affects adversely assimilative and other activ- 
ities, a meager store of nutritive materials would be the result 
of a dry summer, and would find expression the following year 
in reduced growth in length of all the new shoots. Of course 
this weakness of the buds would not occur in trees as a result of 
diminished precipitation in situations providing adequate soil 
moisture throughout the season, but only where drouth appears 
early, as is usually the case on southern and western slopes. For 
this reason those trees in the locality mentioned which grew 
nearer the water level showed no such inequality in the length of 
the internodes, and the same was found to be true in more favored 
situations elsewhere. 

It is true, of course that assimilation can take place at all 
seasons in evergreens, under proper conditions of temperature 
and illumination. It has been shown that assimilation may 
proceed in some plants at a temperature as low as — 40° C., and 
that in pines and spruces the process is active at 3° to5° C. In 
the northern Rocky Mountain region, however, the temperatures 
are considerably below o° C. during most of the winter, and fre- 
quently below — 40°C. The soil, moreover, is frozen to a depth 
of several feet, resulting in a reduction of the water supply. In 
this problem, however, it is chiefly a question of relative activity 
and not of complete suspension of photosynthesis at any time, 
while we are dealing with reserve material in the form of proteid, 
not starch, nevertheless the synthetic activity of the tree, so far 
as this material is concerned, is closely associated with starch 
formation, according to the best evidence at present available. 

Seeking further evidence on the relation of the growth of 
yellow pine to the distribution of rainfall, the writer made two 
series of observations in the vicinity of Missoula, the results of 
which are given in the accompanying tables. Where the forest 


121 


borders on the grass land strips of timber afforded convenient 
material for study. In these cases the stand was a mixture of 
yellow pine and Douglas fir, varying in height from five to 
twenty-five or thirty feet. One of these areas occupies one slope 
of a shallow, narrow valley which traverses in a direction from 
southeast to northwest, the barren western slope of Mt. Sentinel, 
southeast of the town of Missoula. The timbered slope of the 
valley faces the northeast, its opposite slope facing southwest is 
treeless. Along the edge of this stand, a strip over a quarter of a 
mile in length and about fifty yards in width provided the 42 
young yellow pines whose measurements are here recorded. All 
the pines up to thirty feet in height were measured, except such as 
showed evidence of injury in the parts concerned. 

In Table I the height growth is shown of each of the five 
seasons, 1909 to 1913 inclusive. ~The measurements are in inches. 
It will be observed that practically every one of the pines growing 
on this area exhibited a growth during the season of I9II con- 
siderably less than that of either of the two seasons preceding or 
following, and that, although the difference in afew cases is 
reduced to zero, in nearly all of the individual cases the difference 
between the growth of 1911 and that of the other seasons 
amounted to several inches. The same relation appears con- 
spicuously in the totals and again in the averages, but the most 
significant fact seems to be in the absence of exceptions to the 
general rule. 

Table II presents the results of similar measurements on 
another area near Missoula about two miles from the first. Only 
a few observations were recorded in this case, as practically every 
tree approached showed the same condition. 

If one compares these measurements with the weather data 
given in Table III he will find that the lengths of the internodes 
stand in relation to the conditions of the seasons in the manner 
suggested above. The mean precipitation and temperature 


* Miyake, K. On the starch of evergreen leaves, and its relation to photo- 
synthesis during the winter. Bot. Gaz. 33: 321-340, 1902. 

7 Jumelle, Rev. Gen. de Bot. 4: 263, 1892. Pfeffer’s Physiology of Plants, 
Vol. I, p. 338. 

= Green, J. R. Vegetable Physiology, p. 174. IgITI. 


122 


TABLE | 


APPROXIMATE MEASUREMENTS OF THE HEIGHT GROWTH OF Pinus ponderosa, 
MADE ON THE UPPER PORTIONS OF THE MAIN STEM, FOR EACH OF THE 
SEASONS INDICATED, IN INCHES 


No. 1909 IQIO IQir IQ12 1913 
I 8 8 5 6 8 
2 6 8 4 5 6 
3 5 5 4 4 6 
4 IO nme) 6 ume) 10 
5 6 9 3 6 8 
6 8 | 8 5 6 9 
7 9 | 8 8 | 3 8 
8 8 | 6 6 | 5 5 
9 8 | 6 5 9 9 

nae) 13 12 8 Il 13 

II 12 9 8 12 14 

12 7 | 7 5 7 It 

13 8 8 a II 12 

I4 I2 13 Il I4 13 

15 I2 I2 6 sme) 12 

16 4 | 10 6 II | 14 

17 Il | 12 8 12 | 12 

18 | 9 10 7 Il 12 

I9 pit Ii Fl iri I2 

20 I2 =U 6 8 12 

21 10 12 6 Io ime) 

22 I2 12 6 77 9 

23 I4 T4 1K) 15 | I4 

24 I4 T4 II sO) | 12 

25 14 20 6 16 4 

20 I4 IO, 12 IA 4 

27 | I4 10 IO 14 13 

28 13 ies 5 12 13 

20 4 15 IO 13 14 

30 12 13 nO) Wit 12 

31 | Io I4 II 13 I4 

BP II I4 II I4 I4 

BR 13 8 6 | 12 I2 

34 8 8 | 9 | iit 8 

35 IO 13 72 13 I4 

30 | T2 13 | 12 | 12 192 

By | IO II 4 Tey, I4 

38 12 13 9 13 12 

39 13 13 II 14 I5 

40 8 13 9 I2 16 

4I 12 I5 7 13 16 

42 8 8 6 IO 12 

ao caller sae 437 457 2 Bus 443 | A9O 
Average. ....| 10.4 | 10.88 | 7.57 T0.54 | EEOo 


records are given for the months April to September inclusive for 
the years represented by the measurements. The temperature 
is important in this connection as affecting the rate of transpira- 


123 


tion of the trees and the rate of evaporation from the soil. The 
season of 1909 was marked by ample rainfall in June and July, 
and by temperatures, during the earlier part of the season, lower 


TABLE II 


MEASUREMENTS ON THE SAME BASIS AS SHOWN IN TABLE I, BUT OF TREES ON 
A DIFFERENT AREA 


No 1909 IQIo IQII Igt2 1913 
i a6) 50) 9 II 
2 8 Io ai 9 12 
3 10 6 4 5 7 
4 i 8 6 9 9 
5 6 aj 6 8 Ir 
6 7 8 7 Ir IO 
7 7 7 4 8 | 8 
8 7 7 5 8 8 
ANGI S Sia cae 62 63 48 69 65 
Average. .... 7.75 Won 6 8.37 9.28 


than those of any of the other years here recorded. Precipita- 
tion was least in 1910, and of the rain of this season over 40 per 
cent. fell in September, too late to be of much influence in the 
formative work of the year. The months of June and July were 
marked by only four fifths of an inch of rain, and by temperature 


higher than usual, which served to intensify the drouth during 


ANeivis, JUL 
WEATHER DATA FOR MISSOULA, 1909 TO 1913 INCLUSIVE, APRIL TO SEPTEMBER 
T. = temperature, F. 
Ig09 | IgQIoO | IgIt | Igt2 IQI3 
Mo. | ~ i | | | 

| Rain T. | Rain i || Renin eve ekxctin ae Rain AN 
Apr... | I.I9 40 | 0.66 Su |) O74 || 4B | BOR | A | nae 45 
May...| 0.99 SO |) iO x 56 1@O) || Bir BAO). || Sl tei eZ 
iiimeras| 2-05 60 | 0.67 Og |) eager |) TOA |} ae |, Ge 2.39 62 
alive 6 oll S52 Of |) One Wit || Ow |) CO TOYA || (0883 1.52 67 
PAU e ee O:34 66 | 0.57 62 | 0.43 64 TO Cm EOS 1.52 67 
SEDER 2:36 Sy | 27 IO) |) agaae || ea Te OMe O) 0.74 57 
Total . a ILIELO7/ | 6.71 7.05 12.29 8.58 


the very period in which most of the new tissues were taking form. 
This period was followed by another month of dry weather, in 
which the slight amount of rain which fell could have had no 


124 


appreciable influence, and during which the synthetic activity 
of the tree must have been greatly retarded. The year 1911 was 
marked by a more advantageous distribution of the rain, 3.59 
inches falling in June and July, as compared with .8 of an inch 
in the same part of the previous year, and this season’s advan- 
tages were clearly expressed in the ample growth of the shoots in 
the following season. Likewise the season of I912 was an 
exceedingly favorable one for forest vegetation in this region, as 
testified by the excellent growth of all shoots in 1913. 

A series of observations of a similar nature was conducted also 
on the Douglas fir, growing with the yellow pine in the same area 
which furnished the data given in Table I. Twenty-three trees 
were measured, these trees being of about the same age as the 
pines. From the figures given it will be apparent that the com- 


TABLE IV 


APPROXIMATE MEASUREMENTS OF THE HEIGHT GROWTH OF DOUGLAS FIR 
(Pseudotsuga taxifolia), MADE ON THE UPPER PORTIONS OF THE MAIN 
STEM, FOR EACH OF THE SEASONS INDICATED, IN INCHES 


No | 1909 | Igto IgII Igi2 1913 
I | 12 | 13 8 TA 12 
2 6 9 6 II II 
3 | 13 II IO 13 12 
4 13 12 13 I2 Io 
5 II Io I2 I2 I2 
6 13 13 Io I4 I4 
7 4 | 12 8 14 14 
8 Il yy int I4 I2 
9 8 14 13 12 8 

10 | 8 | 05 8 13 I2 

II 13 | 13 13 14 13 

I2 13} I2 12 14 I4 

nz Io | I2 13 I4 I2 

4 12 Io 6 14 i223 

I5 16 12 6 I4 16 

16 12 14 m0) 12 I2 

17 I5 I4 0) I4 I4 

18 9 8 10 12 I2 

19 5 8 6 nae) I2 

20 12 ing 8 nme) 10 

21 12 8 6 13 I2 

22 I4 13 I2 I5 | T4 

23 10 II | 8 8 12 

Moralee see 262 263 219 203 283 


Average. .... II.4 | II.4 9.5 | 12.7 | i snmeoae, 


125 


parative lengths of the internodes are not so uniform as in the 
case of the pines, there being some instances in which the longer 
internode falls in the year 1911, instead of the shorter. The 
reason for these exceptions is not clear; they may possibly be 
due to local variations in the soil moisture. The totals and the 
averages, however, show the same relations to one another as 
in the case of the pines. The figures are given in Table IV. 

It is evident of course that the influence of the preceding season 
is not limited to the retardation of height growth during the year 
immediately following, but that the shorter twigs must involve 
the production of a lesser leaf area than usual, which must in 
turn be reflected in the amount of reserve products accumulated. 
Here, however, the problem becomes complicated, and the 
lessened leaf area on the last shoot may in a measure be compen- 
sated by the greater illumination of the older leaves, by this fact 
made possible. The figures for I912 as compared with those for 
1913 in Table I would seem to indicate the holding over effect 
as here suggested, though the same does not appear to be true 
of the Douglas fir. It is also evident that trees of different 
species on the same areas are not equally responsive to the 
variations of soil moisture in the manner indicated, a fact which 
probably is due chiefly to a difference in the degree of tolerance 
though to some extent to other specific peculiarities. 


UNIVERSITY OF MONTANA 


A NEW SOUTHWESTERN SEDGE 
By KENNETH K. MACKENZIE 


Since writing the article on Carex for the Illustrated Flora two 
species have been found by Mr. E. J. Palmer in southwestern 
Missouri not included therein. One is Carex arkansana Bailey, 
heretofore known from Arkansas and Oklahoma. The other is 
an undescribed species bearing a remarkable outward resemblance 
to the European Carex vulpina L., and in technical characters 
intermediate between that species and our own Carex stipata 
Muhl. It is represented in the collections at the New York 
Botanical Garden by several specimens, and seems first to have 


126 


been collected by Bigelow in 1853-4 in the Whipple Expedition 
from “Fort Smith to the Rio Grande.” Elihu Hall secured it 
on June 6, 1872, in swamps at Hempstead, Texas (No. 734); and 
B. F. Bush collected excellent specimens (No. 993) at Catale, 
Indian Territory, now Oklahoma, on May 22, 1895. These 
specimens in the Columbia University herbarium have been 
taken as the type. Mr. Palmer’s specimens (No. 3405) were 
collected on May 21, 1911, in wet sandy soil near Jasper, Missouri, 
and were distributed as Carex conjuncta Boott. The other speci- 
mens referred to were all distributed as Carex stipata Muhl. 

A detailed description of this species follows, which may be 
known as 


Carex Oklahomensis, sp. nov. 


Culms cespitose, 3.5-8 dm. high, 4-6 mm. wide at base, 1.5 
mm. beneath head, slender but stiff, sharply triangular, rough 
above, not wing-angled or strongly flattened in drying, exceeding 
leaves, aphyllopodic, brownish at base, the rootstocks fibrillose. 
Leaves with well-developed blades 3-4 to a culm, the blades flat, 
thickish, 2.5-5 mm. wide, up to 4 dm. long, serrulate on margins 
towards apex as well as roughened on veins, the sheaths tight, 
strongly green and white mottled dorsally but not conspicuously 
septate nodulose, ventrally white-hyaline not red-dotted or 
cross-rugulose, thin, and soon ruptured, exceeding base of 
blade. Head 4—7 cm. long, about 15 mm. wide, oblong-cylindric, 
with numerous spikes, continuous or somewhat interrupted 
below, the basal branches compound, appressed, sessile or short- 
peduncled, the upper simple, closely aggregated and scarcely 
distinguishable; lower one or two bracts prolonged, setaceous, 
the others scale-like. Spikes androgynous, subglobose, 5-8 mm. 
long, nearly as wide, with some 6-12 appressed-ascending 
perigynia and inconspicuous staminate flowers. Scales ovate 
or lance-ovate, as wide as but shorter than perigynia, chestnut 
brown tinged with hyaline margins and prominent midvein 
excurrent as a cusp. Perigynia lance-ovate, 4-5 mm. long, 1.75 
mm. wide, plano-convex, thick, the walls thin, spongy and sub- 
turgid at base, green or in age greenish-straw-colored but not 
brownish, dorsally conspicuously 7-10 nerved, ventrally less con- 
spicuously fewer nerved, sharp-edged to the truncate sub-cordate 
base, stipitate, tapering to a serrulate deeply bidentate beak 
shorter than body, at apex reddish-brown tinged, and with a 
suture on the outer side. Achenes lenticular, yellow, stipitate, 


127 


ovate-orbicular, 1.75 mm. long, 1.5 wide, apiculate, jointed with 
style, the latter thickened at base. Stigmas two. 


From its American allies this species may be distinguished by 
the combination of wingless culms, erugulose white and green 
mottled sheaths, and beak of perigynium not exceeding body. It 
is to be referred to the group STENORHYNCHAE Holm. 


NEw YORK 


SHORTER NOLES 


TRI- AND TETRACARPELLARY WALNUTS.—In TORREYA, June, 
1913, the writer published a short note on “A Tetracarpellary 
Walnut.” Recently he has had an opportunity to examine a 
series of 106 abnormal walnuts, all from the grove in Santa Ana, 
California, referred toin the first note. Of these 106 walnuts, 89 
were tricarpellary, 45 being symmetrical and 44 unsymmetrical. 
The remaining 17 were tetracarpellary, 7 being symmetrical and 
10 unsymmetrical. The statement as to symmetry is as viewed 
from the pointed end; a few of these specimens were incomplete, 
that is, the grooving of the shell did not extend entirely around 
to the back of the shell. It was not found possible to connect the 
production of these malformed walnuts with any particular tree 
or trees in the grove. 

If this case be taken as typical, it would appear that the 
tendency toward the production of the tricarpellary type is 
greater than that toward the tetracarpellary type, and that ap- 
proximately one half of the specimens are symmetrical or nearly 
so, in both types. 

I am indebted to Prof. R. C. Shuey, of the University of 
Pittsburgh, for these specimens. 

F. ALEX. McDERMoTT. 
MELLON INSTITUTE, 


UNIVERSITY OF PITTSBURGH, 
PITTSBURGH, PA. 


128 


REVIEWS 


Selden’s Everyman’s Garden Every Week* 


Mr. Selden has written a very useful little book which is full of 
information for the amateur gardener. Its introductory chapters 
are upon cold weather planning and reading; saving the family 
purse; garden soils, good and bad; tools that are essential; garden 
eugenics; water whenever needed; garden mistakes of various 
sorts; and taking planting cues from nature. These are followed 
by chapters describing work which may be done to advantage 
during every week from early April until November, and the book 
concludes with chapters on indoor work and suggestions for the 
garden calendar. The book is packed full of suggestions, direc- 
tions and remarks concerning garden crops of all kinds, and cannot 
fail to be of great service to a large constituency. 

N. L. Britton. 


BLACKMAN, V. H. AND PAINE, S. G., A Recording Transpiro- 
meter, Ann. Bot. 28: 109-113, 1914, describe an ingenious device 
for automatically recording the loss of water from a plant. The 
properly prepared potted plant is placed on the left-hand pan of a 
balance and counter-poised. Nearby is a water reservoir with a 
tube placed so as to discharge a uniform series of drops directly 
over an opening in the cover of a flower pot. When the ex- 
periment is started a small vertical funnel, attached to a hori- 
zontal metal tube, intercepts the drops and discharges them into 
a waste vessel. The metal tube passes through two solenoids 
placed end to end.. As water is lost by the plant the left-hand 
balance pan rises and finally, by means of a mercury cup attached, 
makes an electric contact, closing the circuit through the further 
one of the two solenoids. This draws.back the metal tube, and 
water drops now fall into the flower pot. As the left pan descends 
the circuit is broken, but drops continue to fall into the pot until 
the rising right pan, by means of an arrangement similar to that 
on the left pan, closes an electric circuit through the near solenoid, 
thus moving the tube back into its original position. 


* Selden, C. A. Everyman’s Garden Every Week, pp. 1-338, small octavo. 
Dodd, Mead & Company, I914. 


129 


Every time the left pan closes its circuit a portion of the current 
passes through the magnet of a recording pen, marking on a 
revolving drum. The wires with which the mercury cups make 
contact can be raised or lowered, thus varying the interval at 
which the marks are made. The movement of the balance is 
steadied by means of a disc fastened beneath one of the pans and 
moving up and down in a heavy liquid. A number of records 
can be traced simultaneously on the drum, so that it is possible 
to set up two or more plants under different conditions, together 
with an evaporimeter beside every plant and automatically 
record the water loss from each on the same drum. The appar- 
atus is obtainable from Messrs. Baird & Tatlock, Cross Street, 
Hatton Garden, London, E.C. 

It is perhaps asking too much that the fashioners of a beautiful 
piece of apparatus should also present a handsome series of 
results obtained with their invention. Yet it is difficult to repress 
altogether a feeling of resentment in viewing the one puny record 
contributed by the authors. W. G. M. 


i PROCEEDINGS OF THE, CLUB 
FEBRUARY I0, I914 

The first meeting of the Club in February was held February 
10, 1914, at the American Museum of Natural History at 8:15 
P.M. President Harper presided. Twenty-four persons were 
present. Mr. Charles Van Loan’s resignation was tendered to 
the Club and accepted. 

President Harper asked for permission to appoint a series of 
special committees to study the Cryptogamic flora of the vicinity 
of New York. Vice-President Barnhart then took the chair and 
opened the matter for discussion. Dr. Howe made a motion to 
grant President Harper the permission requested. The motion 
was unanimously carried. 

The business program was then followed by an illustrated 
lecture on “The International Phytogeographical Excursion of 
1913,’ by Dr. George E. Nichols. Dr. Nichols will publish a short 
account of the Expedition in Torreya for April. 

Meeting adjourned. MICHAEL LEVINE, 

Sec. pro tem. 


130 


FEBRUARY 25, I914 


The meeting of February 25, 1914, was held in the Laboratory 
of the New York Botanical Garden at 3:30 P.M. President ° 
Harper presided. Twelve persons were present. The minutes 
of February 10 were read and approved. 

The secretary read a communication from Dr. C. Stuart Gager 
relating to the death of Dr. L. Schéney who was at one time a 
member of the Torrey Club. 

The treasurer announced a gift of one hundred and eight dollars 
to the Underwood Fund by Miss Caroline C. Haynes. This gift 
was the proceeds from the sale of ‘“American Hepaticae” (Ex- 
siccatae) prepared and distributed by Miss Haynes. A vote of 
thanks was extended to Miss Haynes for this generous contri- 
bution. 

The first number on the announced scientific program con- 
sisted of a lecture on ‘“‘The Nature and Inheritance of Fascia_ 
tion, by Dr Ol b. White: 

Dr. B. O. Dodge then reported briefly on the use of the stereo- 
scope in connection with binocular microphotographs. 


Adjournment followed. 
B. O. DonGE, 


Secretary. 
MARCH 10, 1914 

The meeting of March 10, 1914, was held at the American 
Museum of Natural History at 8:15 P.M. President Harper 
presided. Twenty-four persons were present. 

The reading of the minutes of the previous meeting and trans- 
action of other business were dispensed with. The announced 
scientific program was then in order. 

Professor H. M. Richards delivered an illustrated lecture on 
“Some Aspects of Californian Coastal Vegetation.”’ 


Adjournment followed. 
MICHAEL LEVINE, 


Sec. pro tem. 
MARCH 26, 1914 
The meeting of March 26, 1914, was held in the Laboratory of 
the New York Botanical Garden at 3:30 P.M. Vice-president 
Barnhart presided. Eighteen persons were present. 


131 


The minutes of the meetings of February 25 and March Io were 
read and approved. Edward D. Hull, 6024 Ellis Ave., Chicago, 
Ill., was nominated for membership. 

The death of Rev. J. Henry Watson and confirmation of the 
report of the death of Dr. C. B. Robinson were announced. On 
the motion of Norman Taylor a committee consisting of Dr. John 
H. Barnhart and Dr. Marshall A. Howe was appointed to draw 
up resolutions on the death of Dr. Robinson. 

Edward D. Hull was then elected to membership. 

The announced scientific program consisted of a paper on 
- “Notes on the Local Flora,” by Mr. Norman Taylor. These 
consisted chiefly of material taken from the introduction to his 
forthcoming work on the “Flora of New York and Vicinity.”’ 

Meeting adjourned. 

BO: DonGeE, 
Secretary. 
NEWS ITEMS 

Dr. Ross Aiken Gortner, who has been in charge of the Bio- 
chemical Laboratory of the Station for Experimental Evolution 
at Cold Spring Harbor, will take up his duties of Associate Pro- 
fessor in the newly established Department of Soil Chemistry 
at the University of Minnesota, August 1. The work in the 
Physico-chemical Properties of Vegetable Saps which he has 
been carrying on with Dr. J. Arthur Harris will be continued 
by his assistant, Mr. John V. Lawrence, and Dr. Harris. 


Miss Susan Minns has given $50,000 to the Botanical Depart- 
ment of Wellesley College, in memory of Susan M. Hallowell, 
the former Head of the Department. 


Members of the Torrey Club are invited to attend a field 
meeting of the American Fern Society to be held July 16, 17 
and 18 in the neighborhood of New York City. A trip to collect 
fern hybrids is contemplated as well as a visit to the New York 
Botanical Garden fern conservatories, and probably also a more 
extended trip for some special fern. Further information may 
be had by writing Mr. R. C. Benedict, 2303 Newkirk Avenue, 
Brooklyn, N. Y. 


132 


Professor Thomas H. Macbride, who has been head of the 
Department of Botany in the State University of Iowa for over 
thirty years, has been elected President of the University. He 
entered upon his new duties April first. 


At a combined excursion of the Torrey Club and several other 
organizations held on June 7, more than sixty people attended. 
The locality visited was Cliffwood, N.J., where the hybrid oaks, 
Quercus Rudkini and Q. heterophylla, were observed, also the 
marl banks there which contain many cretaceous plant remains. 


Dr. J. W. Harshberger will give two courses in systematic 
and field botany this summer along ecological lines at Cold Spring 
Harbor, Long Island, and later on Nantucket. 


The Right Honorable Joseph Chamberlin, who for many 
years maintained one of the best private collections of orchids in 
existence, died July 3, at Prince’s Garden, London. 


We learn from Magazine San Diego that an official in Mexico 
was requested by the governor of the state to render a report 
on the Fauna and Flora of his district. A second more per- 
emptory demand for the delayed report is said to have elicited 
the following: ‘‘Dear Sir: Fauna left this locality two weeks ago. 
Flora is in jail. Awaiting your further instructions, | am, 

‘Your most obedient servant, etc. 
JosE GONZALES.” 


® : 

The Torrey Botanical Club 

Contributors of accepted articles and reviews who wish ‘six 
gratuitous copies of the number of TorrReEya in which their papers 
appear, will kindly notify the editor when returning proof. 

Reprints should be ordered, when galley proof is returned 
to the editor. The New Era Printing Co., 41 North Queen 
Street, Lancaster, Pa., have furnished the following rates : 


2pp App Spp 12pp lopp 20pp 

25 copies $ .75 $1.05 $1.30 $1.80 $2.20 $2.50 
50 copies -90° 1.20 1.70 2.20 2.50 2.85 

~ 100 copies 1.15 1.55 1.95 2.55 2.90 3.20 


200 copies 1.70 2.35 2.90 3.75 4.35 4.70 
Covers: 25 for 75 cents, additional covers 1 cent each. 
Plates for reprints, 40 cents each per 100. 


The following Committees have been appointed for 1914 


Finance Committee Field Committee 


J. H. Barnuart, Chairman ~ SERENO STETSON, Chairman 
Miss C.,C.. Haynes 


Budget Committee Program Committee 
J. H. Barnuart, Chairman -Mrs. E. G. Britton, Chairman 
N: L. Britron Miss JEAN BROADHURST 
B. O. DopGE C. STUART GAGER 
- M. A. Howe F, J.. SEAVER 
A. W. Evans 
Et: H. Russy 


Local Flora Committee 
N. L. Britton, Chairman 


Phanerogams: _ Cryptogams: 
E. P. BicKNELL -Mrs: E. G. Britton 
N. L. Britton PHitre DOWELL 

C. C. Curr®is Tracy E. HAzEn 

K. K. Mackenzie M. A. Howe 
NorMAN TayLor = » Be eA OAS: MURRILG 


pe eat to the Council of the New York Academy of Sciences 
WILLIAM MANSFIELD 


OTHER PUBLICATIONS 


OF THE 


TORREY BOTANICAL CLUB 


(1) BULLETIN 


A monthly journal devoted to general botany, established 
1870. Vol. 40 published in 1913, contained 712 pages of text 
and 26 full-page plates. Price $3.00 per annum. . For Europe, 
14 shillings. Dulau & Co., 37° Soho Square, London, are, 
agents for England. ; 

Of former volumes, only 24—40 can be supplied entire ; cer= 
tain numbers of other volumes are available, but the entire ee 
of some numbers has been reserved for the completion of sets. 
Vols. 24~27 are furnished at the published price OF two dollars 
each; Vols. 28-40 three dollars each. 

ee copies (30 cents), will be furnished only when not 
breaking complete volumes. . 


4 


(2) MEMOIRS 


The Meworrs, established 1889, are published at irregulas 
intervals. Volumes I-13 are now completed ; Nos. 1 and 2 of 
Vol. 14 have been issued. The subscription price is fixed at . 
$3.00 per volume in advance. The numbers can also be pur-, | 
chased singly. A list of titles of the individual papers and ahs 
prices will be furnished on application. 


(3) The Preliminary Catalogue of Anthophyta and Pteri- | 
__ dophyta reported as growiug within one wer miles of New | 
York, 1888. Price, $1.00. 


Correspondence relating to the above publications should be 
addressed to 
DR. BERNARD O. DODGE 
: Columbia Univesity 


New York City” 


A Vol. 14 August, 1914 No. 8 


A Monruty Journat or Boranicat Notes AND News 


4 


EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873 


CONTENTS 


Proposed Work on the Cryptogamic Flora of New York: R. A. HARPER............ 133 
Two New Plants from the Tertiary Rocks of the West: T. D. A. CocKERELL...... 135 


Some Comparisons of the Lichen Floras of Eurasia and North America: 
R. H. Howe, Jr. 138 


A Possible Habit Mutant of the Sugar Maple: A. F. BLAKESLEE..... ......0....002... 140 
A Classification of Botanical Science in Two Dimensions: R. M.-HarPer......... 144 


Ne Wissel terny ss ype) sacs oi ta wk gate slashes ASA OU s oe Sai Feae fo ka heenday sine Babe « Bock ce Apauee a oe 148 


PUBLISHED FOR THE CLUB 


AT 41 NortTH QUEEN STREET, LANCASTER, Pa. 
BY THz\ New Era Printing Company 


[Entered atthe Post Office at Lancaster, Pa,, as second-class matter.] 


THE TORREY BOTANICAL CLUB 


OFFICERS FOR 1014 


Prise: 
R. A. HARPER, PH.D. 
Vice-Presidents 
JOHN HENDLEY BARNHART, A.M., M.D. 
HERBERT, M. RICHARDS, S.D. 


Secretary and Treasurer 


BERNARD. O. DODGE, Ph.D. 
Columbia University, New York City 


Editor 


ALEX. W. EVANS, M.D., PH.D. 
Associate Fditors 


JEAN BROADHURST, Pu.D. MARSHALL AVERY HOWE, Px.D 
ERNEST D. CLARK, Pxu.D. HERBERT M. RICHARDS, S.D. 
J. A. HARRIS Pu.D. ARLOW B. STOUT, PH.D. 


NORMAN TAYLOR 


- Torreya is furnished to subscribers in the United States and 
Canada for one dollar per annum; single copies, fifteen cents. To 
subscribers elsewhere, five shillings, or the equivalent thereof. Postal or 
express money orders and drafts or personal checks on New York City 
banks are accepted in payment, but the rules of the New York Clearing 
House compel the request that ten cents be added to the amount of any 
other local checks that may be sent. Subscriptions are received only 
for full volumes, beginning with the January issue. Reprints will be 
furnished at cost prices. Subscriptions and remittances should be sent 
to TREASURER, TORREY BoTANICAL Cius, 41 North Queen St., Lan- 
caster, Pa., or Columbia University, New York City. 

Matter for publication, and books and papers for review, should 

be addressed to 


NORMAN TAYLOR 


Brooklyn Botanic Garden 
Brooklyn, N. Y. 


fA gS es See al ae 


TORREYA 


August, IgIq4. 
Vol. 14 ; No. 8 


PROPOSED WORK ON THE CRYPTOGAMIC FLORA 
OF THE REGION ABOUT NEW YORK 


May 8, 1914 


To THE MEMBERS OF THE TORREY BOTANICAL CLUB: 


The following program for work on the cryptogams has been 
sent to all members of the Torrey Botanical Club and others 
interested. It is desired to secure the coéperation of as many 
collectors and field workers as possible. 

The Club proposes to undertake special work during the 
coming year on the cryptogamic flora of the region. The com- 
pletion and provision for publication of Mr. Taylor’s list of the 
flowering plants and ferns suggest the extension of the Club’s 
activities to this further field as the next large undertaking 
necessary to complete our knowledge of the plant life of the local 
flora district. 

Notable work on various groups of the cryptogams has already 
been accomplished and it is hoped to publish at once in the 
Club’s journals preliminary lists, so far as they are available. 
It is the desire of the Club to enlist the assistance in this under- 
taking of as many collectors and field workers as possible. It 
has been decided to create a considerable number of special 
committees with chairmen, who, as far as possible, are interested 
in particular groups and to invite the members of the Club and 
others to enroll themselves on one or more of these committees. 
The chairmen will organize field excursions either for their 
special work or in conjunction with other committees and the 
effort will be made to arrange the dates for trips to the different 
regions so as to visit each locality at a time most favorable for 


_ [No. 7, Vol. 14, of TORREYA, comprising pp. 115-132, was issued 17 July 1914.] 


133 


134 


collecting its special flora. It is desired that the data obtained 
should include records as to abundance, perfection of develop- 
ment, etc., at the various stations for each species and that such 
records be continued in succeeding years so that in the case of 
the fleshy fungi and algae, especially, more reliable information 
as to their occurrence and distribution than is now available 
may be accumulated. 

Facilities for domparing, identifying and preserving material 
will be provided at the New York Botanical Garden, the Brooklyn 
Botanic Garden, Columbia University, Barnard College, Yale 
University and Rutgers College. 

The excursions for the study of the flowering plants under Mr. 
Stetson will also be continued as heretofore and members are 
asked to enroll themselves for this work as well as for that on 
the cryptogams. 

You-are cordially invited to enter your name under the head 
of one or more of the committees named and to return the en- 
closed slip to B. O. Dodge, Secretary of the Club. Notices as 
to special meetings, field trips, etc., will then be sent to you 


from time to time. 
R. A. HARPER, 


President 
Ba (OL IDs, 


Secretary 


CHAIRMEN OF SPECIAL COMMITTEES ON LOCAL FLORA, 
TorRREY BOTANICAL CLUB 


loweninegiulambse: wee. ccc fae ive me one usu oee ae Sereno Stetson 
ers andahienaealllies, 077 3025 Mie eset | R. C. Benedict 
INTOSSES Sty erreinbe Cait cl eens Lene eee Mrs. E. G. Britton 
PAVE W OLUS ree e Ce ss et eee och ene a fey eee cena ne ae A. W. Evans 
Binesin Wiatene nledewe cs). oo... a ee 2 pak. Ee alazen 
Nantne sal caer tere fc eo). ta pee ee eee . «MAP Howe 
Gasteromlycetes see te ee i ee pone 
FAW AMETIOMIVCCUCS eee cei aire Serine een Ae ee W. A. Murrill 
Except Russula and Lactarius... .. .Miss G. S. Burlingham 


Gortinanusryers tet es oo ee ee ee Scenery eae R. A. Harper 


Okymorcacins: | oo e seme mre Se Oy bis M. A. Levine 
“2 SG] SC UT pai e ea eke  P i  e anna H. M. Richards 
Rusts and Smuts.:...... lo EEG BR a ee E. W. Olive 
Descomycetesicy. Wa ME ea, B. O. Dodge 
Peter Ves Se et a Ree, Oh W. C. Barbour 


Pyrenomycetes, Sphaeriaceae and Dothideaceae.H. M. Richards 
Hypocreaceae, Perisporieae, Plectascineae, Tuberineae, 


a. jie) Seaver 
Reb ORIMITIS SClCT@tIAn nee. See ee es eo A. B. Stout 
Imaperfecti........ H. M. Richards, F. J. Seaver, Mel T. Cooke 
(OTIC SUES Soe ce tine at ee ek er a C. A. King 
MRP UNIAN ER LES che caso ta ere hae, Mey ode A. F. Blakeslee 
MBbmrgnsantaceae sal fons Ce oy ye le es 
WD ivexOMIVGELES 2). ola de sn eek ey ee nd bese Miss M. E. Latham 
Wescisrand: Bacteria. f!2.an.: 2321.22) 25.-% Miss J. Broadhurst 
Lipecerete, (Geen sae aa ei tare ara rea eg Mel T. Cooke 


DVO NEW PLANTS FROM THE TERTIARY ROCKS - 
. OF THE WEST 


By T. D. A. COCKERELL 
Smilax labiduromme sp. nov. 


Leaf 53 mm. long and 35 wide; deltoid, with truncate base, 
the lateral margins nearly straight, but under a lens showing 
shallow crenulation; five principal longitudinal veins. 


Miocene shales, Florissant, Colorado, Station 14 (Wuzlmatte 
P. Cockerell). On the same slab, three mm. from the leaf, is an 
earwig, Labiduromma bormanst Scudder. The genus Smilax and 
the family Smilaceze are new to the Florissant list, but various 
species of Smilax have been found in other American formations. 
Smilax carbonensis n. n. (S. grandifolia Lesq., Tertiary Flora, 
Pl. [X, f. 5, from Carbon, Wyoming) is a larger leaf, with cordate 
instead of truncate base, and convex lateral margins. It is 
probably quite distinct from Smulacites grandifolia Unger,* 
which as originally figured by that author, has the basal sinus 
very deep (over 30 mm.); and in any event S. grandifolia Buck- 


* Chloris Protogaea, pl. XL, f. 3. 


136 


ley* antedates Unger’s name by about four years. In the 
determination of Smilax leaves there is indeed a large element of 
uncertainty, owing to the variation in outline, as Laurenty 
has beautifully illustrated in the case of S. aspera. This should 
prevent us from multiplying specific names based on different 


Fic. 1. Smilax labiduromme Cockerell. 


looking leaves of the same region and period, but on the other 
hand, it should not lead us to consider identical plants of quite 
different parts of the world and different geological horizons. 
Something must be allowed for the inherent probabilities in 
each case. Knowltont has described Smilax lamarensis from the 
supposed Miocene of the Yellowstone; it resembles S. carbonensis 
rather than the Florissant species, having the cordate base and 
rounded sides. Heer,§$ from beds supposed to be Miocene at 
Asakak, Greenland, describes a Smilax lingulata; it is a narrow 
leaf quite unlike the Florissant plant, resembling, in fact, the 
living S. laurtfolia L. 

A much more ancient plant assigned to this genus is Smilax 

* Am. Journ. Sci. 45: I7I. 1843. 

7 Ann. Mus. Marseille, 12: pl. 1. (1908.) 


t Geol. Yellowstone Nat. Park, pl. CXXI, f. 3, 4. 
§ Kong]. Sv. Vet. Akad. Handl., 13, no. 2: 15, pl. 1, f. 12 (1874). 


137 


Kansana n. n. (S. undulata Lesq.,* not of Pohlt), from the 
Dakota group in Kansas. 


Tithymalus phenacodorum sp. nov. 


Seed. Length 4.75, breadth 4.25 mm.; short-pyriform, with 
four sides slightly flattened; surface coarsely irregularly wrinkled. 
Five miles southeast of mouth of Pat O’Hara Creek, Clark’s 
Fork Basin, Wyoming; above red-banded beds, in strata sup- 
posed to be older than the Wasatch, though formerly classed 


Fic. 2. Seeds of Tithymalus: A. T. prenacodorum, side view. B. T. phenaco- 
dorum, from above. C. T. Willistoni, side view. 


with that group. Typein American Museum of Natural History; 
collected by Mr. W. Stein, along with numerous remarkable land 
shells, of the genera Protoboysia, Boysia, Vitrea, Thysanophora, 
Pyramidula, Gastrodonta and Oreohelix. 

Compared with the seeds of T. Willistont Cockerell,? from the 
Loup Fork Beds of Long I., Kansas, the new species is distinctly 
longer, while the depressions between the ruge are more irregular 
and less definitely in longitudinal series. A quite similar but 
still longer seed is that of the living Mexican Tithymalus 
campestris n.n. (Euphorbia campestris Cham. & Schl., 1830), the 
seed of which is well figured by Millspaugh, Botanical Gazette, 
XXV (1898): 25. In TJ. campestris, however, the rugae are 
more labyrinthiform than in T. phenacodorum. 

Extremely hard and dense seeds, such as those of Tithymalus, 
are readily fossilized where ordinary vegetation decays and 
disappears. It is probable that careful search will reveal them 
in other Tertiary strata. I adda figure of T. Willistont, as it has 
not been figured. 

* Fl. Dakota Group: 39 (1892). 


7 Pohl, A. DC. in D. C., Mon. Phan. 1: 135. 
i Torreyag: II19. 1909. 


138 


SOME COMPARISONS OF THE LICHEN FLORAS OF 
EURASIA AND NORTH AMERICA 


By R. HEBER HOWE, Jr. 


In studying many of the filamentous and foliose lichen-species © 
of North America I have been struck with the interesting corre- 
lation of species-distribution found on the two continents of 
North America and Eurasia. This correlation is so often over- 
looked, that new varieties and even species are being described 
without a sufficient study of the distributional problems that 
present themselves, though as Dr. Darbishire has pointed out, 
these species may be ‘‘alike only in their external morphology,”’ 
and “ 
ancestor.’ It, nevertheless, should make one wary of describing 


may have been separately derived from some common 


new species even if excused by any such theoretical probability. 

That the lichen flora of western Europe and the western 
coast of North America is closely allied,—as that of eastern 
Asia and eastern portions of the United States is, in some striking 
instances, at least undeniable. I am told that the same analogy 
is apparent in other groups, 7. e., the mosses.* 


CLIMATE, ELEVATION, ETC. 


There are evidently several underlying causes that develop 
lichen species; just what these are, and their relative importance, 
is still to be explained. We have climatic conditions, the three 
most important factors of which for lichens, as for all plants, 
are moisture and sunlight, and the variability of temperature 
due to elevation or latitude. The character of the soil (of no 
concern in the species here discussed) plays, no doubt, an im- 
portant réle. The proximity of the sea also, it would seem, 
has a definite influence. All of these factors, however, fail, it 
appears, to explain entirely the curious occurrence of a given 
species on both continents. A combination of them all is more 
likely the answer. 

[* Gray, Hooker and many recent writers have discussed the well-known rela- 


tionship of the flora of eastern Asia and eastern North America. See TORREYA 
for January 1914, p. 8.—Ed.] 


139 


In a recent paper by Dr. Darbishire* on Arctic flora, a most 
interesting and enlightening comparison of Arctic species with 
those of Germany is made, showing that the advance and 
retreat of the ice age explains a remarkable distribution, which 
results in 72.3 per cent. of Arctic lichens being found in the Tyrol. 
A conclusion, that the crustose species are of a later evolutionary 
development than the fruticose, is also brought forward by means 
of comparison of the two floras. 

A few examples taken from the Usneaceae show the correlation 
that I have in mind, and which at a later date I moigle to be able 
to take up in more detail. 


Genus: USNEA 


U. plicata (L.) Web. I have before me examples of Usnea 
plicata from the Alps which are practically as robust as those 
from the Californian coast, and are impossible to separate if 
the labels are withheld. These Californian plants have been 
described as representing a new species, 7. e., U. californica 
Herre. This species was considered by Dr. Zahlbruckner to 
belong to the series Pachynae, but in reality it is a Mesinae, a 
point in which Dr. Zahlbruckner now agrees with the author.f 
Dr. Herre was perhaps mislead by this belief when he described 
the species. 

U. articulata (L.) Hoffm. Though this species is never well 
developed in our area, it is found only on the Californian coast. 
It is of course a well marked species in the British Isles. 


Genus: LETHARIA 


L. vulpina (L.) Ach. This plant occurs throughout north- 
western United States, reaching in California perhaps, a slightly 
more robust development (7. e., L. vulpina var. californica 
Nyl. = L. columbiana Nutt.) and is an exactly parallel case with 
U. plicata. 

* Rept. 2d Norwegian Arctic Exped. ‘‘Fram,’’ 1898-1902, Videns. Sels. I Krist. 
51-53. 1909. 

7 In litt. Sept. 9, 1913, ‘‘ Die californica, deren Originale exemplar bei mir erliegt 


ist eine echte Pachyna.” In litt. Feb. 2, 1914, “Darin haben Sie recht, dass Usnea _ 
californica nicht zu des Pachynae gehort.”’ 


140 


L. thamnodes (Flot.) Hue. This species shows that the 
eastern Asiatic distribution is in this case parallel with that of 
eastern United States. L. thamnodes is not known from west of 
the Mississippi and is now considered synonymous with Evernia 
mesomorpha Ny. from eastern Asia. 


Genus: RAMALINA 


Ramalina fraxinea (L.) Ach. This species (typica) is unknown 
from our area except on the Pacific coast, and we have small 
argument to distinguish it from the common R. Mensiezit Tuck.,— 
in fact unlabelled material from the coast of France is in many 
cases impossible of separation (see Bryologist 17: 20-22. 1914). 

R. Duriaei (DeNot.) Bagl. This plant occurs only in southern 
California and appears again on the southeastern Atlantic coast 
of Europe. 

R. calicaris (L.) Fr. emend. (= scopulorum). The only repre- 
sentative of this species-group is the occurrence in Alaska of 
“R. subfarinacea Nyl. 


- Genus: ALECTORIA 


A. Fremontit Tuck. This species, known only from western 
North America, is no longer a unique representative of our area, 
as it is now well known from Scandinavia and even France. 


THOREAU MUSEUM OF NATURAL HISTORY, 
ConcorbD, Mass. 


A POSSIBLE HABIT MUTANT OF THE SUGAR MAPLE 
(ACER SACCHARUM)* 


By A. F. BLAKESLEE 


In the summer of 1911 while on a collecting trip near Bing- 
hamton, N. Y., the writer’s attention was attracted to a single 
tree in a distant row of sugar maples. Its strikingly regular 
outline suggested either that it had become overgrown by a 
vine or had been artificially trimmed to suit the whim of some 
topiarian artist. A closer approach and inspection, however, 


* Contribution from the Department of Genetics, Connecticut Agricultural 
College. 


141 


showed that neither supposition was correct. Moreover, the 
owner of the farm upon which the tree was growing, Mrs. Lucy 
A. Burbank, gave the information that the tree in question had 
been planted by her husband somewhat over 30 years pre- 
viously, together with the other trees seen in the row (Fig. I). 
The exact source of the young trees could not be given but, when 
planted, all were supposed to be normal sugar maples. It had 
early shown its peculiar form and most people who had seen it 
insisted it had been kept trimmed, but such was not the case. 
A comparison with the adjacent trees of the same age would 
indicate that its growth had been relatively slow. At the time 
the photographs were taken, its height was about 32 ft. and 
the diameter of the trunk at breast height was 9 inches. For 
comparison it may be stated that the height of the first tree to 
the right of the one in question is about 43 ft. and has a trunk 
diameter of 15 inches. 

The limbs are slender and branch profusely to form a close 
thicket of slender branchlets which end at a nearly uniform 
distance from the trunk. By the shortness of the petioles of the 
outer leaves and the progressive elongation of the petioles of 
those toward the base of the season’s growth, the foliage is 
formed in a dense, even thatch which, in connection with the 
regularity of the skeleton, produces an appearance similar to 
that of a symmetrical arbor vitae. So far as can be seen, the 
habit of growth alone is peculiar, for the individual leaves and 
winter twigs are like those of normal sugar maples. 

Scions have been sent to the New York Botanical Garden and 
to the Arnold Arboretum. Successful grafts onto normal stock 
have been obtained at the latter institution as well as in the Bo- 
tanic Garden of the Connecticut Agricultural College. Without 
doubt the tree will hold its peculiarity of growth when propagated 
vegetatively as have other form varieties of maples such as the 
fastigiate sugar maple (var. monumentale) which has the aspect 
of a Lombardy poplar. 

A short note describing this habit variant of the sugar maple 
was presented at the Washington meeting of the Botanical Society 
of America, I911, and an abstract of this note was given in 


142 


Science, Jan. 26, 1912. Since then two trees of somewhat similar 
appearance have been brought to the writer’s attention. 

Under date of Jan. 29, 1912, Mr. J. N. Prouty of Humboldt, 
Iowa, writes: ‘We have in this town what I presume is a dupli- 


Fic. t. Summer and winter view of possible habit nutant of sugar maples. 


cate of your tree. . . .. The tree is more than 40 years old, the 
stem about one foot in diameter, and more than 30 feet in height 


143 


though it has the appearance in the picture of being a shrub. 
It was transplanted with many others of the same variety to a 
gravelly ridge where it made a slow growth—slower than the 
one to the right which is of the same variety and transplanted 
at the same time.’’ A colored photo postal sent shows a bushy 
tree of regular outline much broader than the one pictured in the 
present article. Those “‘of the same variety’’ in the row are 
obviously normal sugar maples. 

Mr. L.S. Hopkins, of the Peabody High School, Pittsburg, Pa., 
after examining photographs sent him, writes concerning a tree 
discovered in Wayne, Co., Ohio: ‘Although of a slightly differ- 
ent type, I think my tree is exactly the same. . . . The tree is 
not an unusually large one but rather undersized. However, 
the shape is such that every one who sees it for the first time 
thinks it has been trimmed into its present form but so far as I 
have been able to find out it has never been touched.”’ 

The three trees discussed, in addition to their regularity of 
outline, show in common a relatively slow growth. The wide 
separation of the localities where they are found would indicate 
they had originated independently. It is possible that individual 
trees of similar habit may be found in other localities. If so, 
the writer would be glad to have them brought to his attention. 
The form, however, is so unusual in a deciduous tree and so 
conspicuous from a distance that it is improbable they could 
escape notice, even of a layman. Their occurrence therefore 
must be extremely rare. Moreover, Prof. C. S. Sargent has 
kindly examined photographs of the tree from Binghamton, 
N. Y., and informs the writer that no occurrence of a sugar 
maple with any such habit of growth has been reported or is 
known in the literature. 

Fruit has not been obtained from any of these three trees and 
the writer has been unable to visit the tree at Binghamton 
during the flowering season. In consequence no experiments 
have been undertaken to discover how the peculiar form is 
inherited in sexual reproduction. That the peculiarity is an 
inheritable character and not a mere environmental modification 
is presumable from the association of the abnormal forms with 


144 


normal trees acting as controls under similar growth conditions. 
The term mutation may be conveniently applied to the sudden 
appearance of an inheritable peculiarity, whether due to an 
immediately preceeding change in the germ plasm or to the rare 
kaleidoscopic combination of unit characters already present. 
The form variant of the sugar maple here described therefore, 
may be provisionally classed as a mutant. 


A CLASSIFICATION OF BOTANICAL SCIENCE IN TWO 
DIMENSIONS 


By ROLAND M. HARPER 


The classifications of knowledge relating to the vegetable 

kingdom which one finds in encyclopedias, text-books, library 
manuals, etc., usually arrange the ultimate units in a linear 
sequence (a space of one dimension), and almost necessarily so, 
for the parts of a written or spoken discourse, such as a lecture 
course, are consecutive rather than simultaneous. But a classi- 
fication of science, books, plants, life-zones, or anything else, 
that has but one dimension can not as a rule place all the units 
in their proper relation to each other, for in a linear sequence 
each unit can be adjacent to not more than two others.* 
_ An ideal classification should have several dimensions, but 
any system represented on a sheet of paper or other plane surface 
is limited to two. This answers fairly well for classifying sci- 
ences, though, for it allows us to classify them by subject matter 
and by point of view at the same time. 

The subjoined table represents a crude attempt to arrange the 
botanical sciences in two dimensions. The columns represent 
the objects studied, and the horizontal divisions the points of 
view or methods of investigation. The columns form a regular 
series of increasing complexity, from vegetable matter in general 
to plant associations; but there is no such simple relation between 
the horizontal rows, and if a third dimension were available the 
points of view might advantageously be grouped in two dimen- 
sions instead of one, so as to bring the study of environment, 


* One of the latest and most elaborate linear classifications of pure and applied 
botany is that of Harshberger in Science, II. 36: 521-525. Oct. 18, 1912. 


145 


TABLE OF BOTANICAL SCIENCES 


Objects ||__. A : 
F ssocia- 
Points Vegetable \ells Tissues | Organs | Plants Lion 
of view matter 
\} | | 
General (func- | | ie Bid 
tions, classi- || Botany | Cytology | Histology) oe peas I Sociology 
fication, etc.) | ee 
| | 
, || Plant | 
j | ‘ oy? >? 
Composition | chemrsuiay Pharmac ology? F 
{| pis ieee wl 
: || Specific | ‘ Strength 
oye ti gravity peu of wood, ® 
pEQpeTtics ete. P etc. 
Structure | Mo; rp h q i © gy ? 
Nutrition, 
respiration, | SDA : 1 # | 
photosyn- {| Meas) 2s o Oss a7 | 
thesis, etc. | | 
ST | | | 
Germination || 
and growth, | Rib ye sitios 0 2-7: invasion? 
or life history || | | 
| 
Seasonal or | : 
arierran il | 1 | 
other periodic || SS AS LLL 2 
Phenol ogy 
changes 
co a || | 
Movements and | Phage olleesy 
responses | 
Reproduction ES a 
ology | 
| | 
Pesca: er | Genetics | 
inheritance 
| | | 
| | | Phyl- | 
Evolution or | > ogeny | Suc- 
history 3 Paleo- cession 
botany 
| Compe- 
tition 
Interrelations ? ? Syl 2OREN SL 
osis, etc. 
parasi- 
tism,ete. 
Environment oe Par hs Synec- 
(influence of) BY ology 
Areal 
distribution eo 2S 


146 


for example, next to that of seasonal changes’ and movements 
and responses, as well as to interrelations and distribution. 

The rectangular spaces left blank are those in which no laws 
can be placed. For example, we can hardly conceive of the 
nutrition of plant associations, or the geographical distribution 
of cells. Spaces occupied only by interrogation points are 
those in which there seem to be a few laws, but not enough to 
have received a special name as yet. 

The last four or five columns should each be regarded as made 
up of a multitude of smaller ones, corresponding to the different 
kinds of tissues, plants, etc. Organs can be subdivided twice, | 
first into kinds of organs, and then into different forms of each 
kind. Plants may be classified either by their supposed phylo- 
genetic relationships, as in taxonomy, or by structure and 
adaptations (this sometimes called ecological classification), or 
in various other ways. For the taxonomic subdivisions there 
are numerous minor “‘-ologies,’’ such as mycology, bryology, 
agrostology, and even batology and ionology; and for the struc- 
tural subdivisions there are a few terms, of which dendrology is 
probably the most familiar. 

Some of the horizontal rows, especially the last two, can be 
similarly subdivided. The subdivisions of ecology are the 
various environmental factors, and those of geography the 
divisions of the earth’s surface; and each of these systems may 
be arranged in more than one way. 

In studying any portion of the field we may proceed either by 
rows or by columns. For example, most ecological treatises use 
the environmental factors for the primary subdivisions, and 
consider the effect of each one separately on organs, plants, etc. 
But the Chicago text-book, published about two years ago, 
considers the organs first, and then the relation of each to different 
environmental factors. Each method of course has its advan- 
tages. 

In a general way this table might be said to indicate the order 
of historical development of the sciences named. If such a 
table had been prepared in the time of Linnaeus it would prob- 
ably have lacked most of the lower half. The last column and 


147 


the last row but one received very little recognition anywhere 
until the last decade of the nineteenth century (and even yet 
very little attention has been paid to them in some of the 
older states where botanists are most numerous). 

The best order for teaching these sciences in a complete 
botanical course—if such a course is ever given—is not so 
obvious, principally because a course of instruction cannot very 
well proceed in two directions simultaneously, but must follow 
rows, or columns, or first one and then the other. ‘Perhaps the 
best way around this difficulty would be to subdivide the field 
along horizontal lines into several parts, and then take a column 
at a time, transgressing the upper or lower limits occasionally 
to make certain points clearer. Then too it is customary to 
teach along with the pure sciences more or less of certain applied 
sciences or arts which have no place in the table, such as eco- 
nomic botany, forestry, plant breeding, and agriculture. 

It will be observed that systematic botany or taxonomy, 
which was once the largest feature in botanical text-books, is 
absent from the table. Classification is not peculiar to plants 
or organisms of any kind, and in itself is not a science at all, but 
rather an art, a method or a convenience. The earlier classi- 
fications of plants were very artificial and not scientific, but the 
scientific basis of modern taxonomy is phylogeny, which has its 
proper place in the table. 

Some botanists are inclined to regard physiology and ecology 
as essentially one, while others have difficulty in drawing the 
line between ecology and geography.* But the above table and 
explanation should make the relations between these three 
sciences clear. Although they are more or less interdependent, 
they consider plants from three fundamentally distinct points of 
view. Plant sociology, which is sometimes regarded as a part 
of ecology, is still more distinct. 

It is scarcely necessary to remark that the sciences dealing 
with the animal kingdom in general and those dealing with man- 
kind in particular could be classified in a very similar way. 


* Human ecology and human geography have been even more persistently 
confused than the corresponding botanical sciences, and a great deal of modern 
so-called geography is nothing but ecology. For additional notes on the scope of 
geography see Science II. 38: 816. Dec. 5, 1913. 


148 


NEWS ITEMS 


On July 16, the Torrey Club and the Staten Island Asso- 
ciation of Arts and Sciences were entertained by Dr. N. L. 
Britton and his brother, Mr. R. H. Britton, at Great Kills, 
Staten Island. The party, numbering over sixty, were taken in 
motor-boats over to Crooke’s Point where the flora was observed. 
Dinner was served at a local hotel at which speeches were made 
by Dr. Britton, Professor Harper, Dr. Hollick, Messrs. Cleaves 
and F. D. Tansley, and others. In the afternoon further explora- 
tion of the region was enjoyed by the party. 


According to a careful census just completed, the Botanic 
Garden of Grinnell College, Iowa, with the adjacent nursery, 
reports 494 distinct species and hybrids, mostly of hardy plants, 
and 115 minor varieties and forms. The uncultivated part of 
the garden contains probably 50 other native and naturalized 
species. 

Dr. R. M. Harper is at work on a study of the geography and 


vegetation of northern Florida. His address until September 
first is Florida State Geological Survey, Talahassee, Fla. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six 
gratuitous copies of the number of Torreya in which their papers 
appear, will kindly notify the editor when returning proof. 

Reprints should be ordered, when galley proof is returned 
to the editor. The New Era Printing Co., 41 North Queen 
Street, Lancaster, Pa., have furnished the following rates : 


2pp 4pp 8pp 12pp 16pp 20pp 
25 copies $ .75 $1.05 $1.30 $1.80 $2.20 $2.50 
50 copies -90 1.20 1.70 2.20 2.50 2.85 


-100 copies 1.15 1.55 1.95 2.55 2.90 3.20 
200 copies 1.70 2.35 2.90 3.75 4.35 4.70 


Covers: 25 for 75 cents, additional covers 1 cent each. 
Plates for reprints, 40 cents each per 100. 


The following Committees have been appointed for 1914 


Finance Committee Field Committee 
J. H. Barnuwart, Chairman SERENO STETSON, Chazrman 
Miss C. C. HAYNES 
Budget Committee Program Committee 
J. H. Barnuart, Chairman Mrs. E. G. Britton, Chairman 
N. L. Brirron Miss JEAN BROADHURST 
B. O. DopGE C. SruarT GAGER 
M. A. Howe F, J. SEAVER 
A. W. Evans 
H. H. Russy 


Local Flora Committee 
N. L. Britton, Chairman 


Phanerogams: Cryptogams: 

E. P. BIcKNELL Mrs. E. G. Britron 
N. L. Britton Puitrie DowELL 
C.-C. Curtis Tracy E. Hazen 

K. K. Mackenzie M. A. Howe | 
NorMAN TAYLOR W. A. MurriLy 


Delegate to the Council of the New York Academy of Sciences 
WILLIAM MANSFIELD 


OTHER PUBLICATIONS 


bars THE 


TORREY BOTANICAL CLUB 


(1) BULLETIN 


A monthly journal devoted to-general botany, established 
1870, Vol. 40 published in 1913, contained 712 pages of text . 
and 26 full-page plates. Price $3.00 per annum. For Europe, 
14 shillings. Dulau & Co., 37° Soho Square, London, ‘are, 


agents for England. 


_ Of former volumes, only 24—40 can, be supplied entire; cer- 
tain numbers of other volumes are available, but the entire stock — 
of some numbers has been reserved for the completion of sets. 
Vols. 24-27 are furnished at the published price of two dollars 
each; Vols. 28-40 three dollars each. 

Single copies (30 cents) will be furnished only when not 
breaking complete volumes. | 


(2) MEMOIRS 


The Memoirs, established 1889, are published at irregulas 
‘intervals. Volumes 1-13 are now completed ; Nos. 1 and 2 of 
Vol. 14 have been issued. The subscription price is fixed at 
$3.00 per volume in advance. The numbers can also be pur- 
chased singly. ‘A list of titles of the individual papers and of 
prices will be furnished on application. 


(3) The Preliminary Catalogue of Anthophyta and Pteri- 
dophyta reported as growing within one hundred miles of = Pe 
York, 1888. -Brice, $1.00. ; 


Correspondence relating to the above publications should be 
addressed to 
DR. BERNARD O. DODGE 
Columbia University 


‘New York City 


Vol. 14 September, 1914 No. 9 


TORREYA 


A Monruty Journat or Boranicat Notes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-1873 


CONTENTS 


The Aquatic Vegetation of Squaw Shoals, Tuscaloosa County, Alabama : 
R. M. HARPER 149 


A new southeastern sedge: K. K. MACKENZIE... 02. .....cccecececceeceee, cececcueneeseueccess 155 


Additions to the Pleistocene flora of the southern states: E. W. BERRY............ 150 

_ Shorter Notes 
Occurrence of Indian Pipe: J. J. DAVIS........ oii. cecceecececece ceeeeeee is saree iD 162 
““Modern”’ Botany in 1821.2 -..... 6.0 ..ccccepeceneeee ie idee Re San, Bes seh ass atete toes 162 
Proceedings of the Club......... racist Ruse ESE TD), Sere cane Ope lls Oe NK, Pete ea 163 
A Wews: Ttems.o. 20 cys fr... z. ad aS LD Tae ca Ee gO AM AN ee See SA ca 165 


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3 NORMAN TAYLOR 


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ree 1914 


TORREYA 


. September, IgI4. 
Vol. 14 : No. 9 


THE AQUATIC VEGETATION OF SQUAW SHOALS, 
TUSCALOOSA COUNTY, ALABAMA 


By RoLAND M. HARPER 


Most rivers which traverse hilly and rocky regions have rapids 
or shoals at many places, where they cross strata a little harder 
than the average. At such places the gradient of the stream-bed 
is steeper than usual, and consequently the velocity of the water 
is greater and its depth and seasonal fluctuations less. Most 
rocky shoals, in the eastern United States at least, seem to be 
almost devoid of aquatic vegetation. But for some reason not at 
present obvious, vegetation seems to thrive on the shoals of the 
Warrior River, which drains most of the coal region of Alabama 
and parts of some of the neighboring limestone valleys. Shoals 
were formerly abundant along this river and its tributaries above 
the fall-line at Tuscaloosa, but in the last two decades all within 
25 miles of Tuscaloosa have been obliterated by the building of 
locks and dams for the purpose of extending navigation to as 
many coal mines as possible and ultimately to Birmingham 
(‘the Pittsburgh of the South’’). The lowest shoal on the river 
that is still visible is Squaw Shoals, in the extreme northeastern 
part of Tuscaloosa County (in T.18S., R. 8 W.), about 26 miles 
from Tuscaloosa by water. And at the present writing a 63-foot 
dam (Lock 17) is being built at its foot, which if no unexpected 
difficulties arise will completely spoil the shoals for scientific 
purposes within a year or two.* 

* Since the above sentence was written the work has been suspended for lack 
of further appropriations from Congress, which will be welcome news to phyto- 
geographers. 


{No. 8, Vol. 14, of ToRREYA, comprising pp. 133-148 was issued 12 August 1914.] 


149 


150 


On a visit to Squaw Shoals on June 4, 1913, I gathered some 
facts which may be of interest for comparison with other places, 
even after the opportunity for verifying some of them is gone 
forever. Se ore 

The shoal is about three miles long and a thousand feet wide, 
with a total fall, at low water, of forty feet. Its foot is about 1 55 
feet above sea-level. As some of the accompanying illustrations 
show, the river in this part of its course is bordered by rather 
steep wooded hills, rising two or three hundred feet above the 
water in a distance of half a mile or so, but the country is not at 


Fic. t. View of Squaw Shoals looking up-stream, showing Dianthera in fore- 
ground and Panicum virgatum farther away. The most conspicuous trees at the 
brow of the bluff at the right are Pinus palusiris. 


all mountainous. The rock in the neighborhood is all shale 
and sandstone of the upper Carboniferous, with the strata hori- 
zontal or nearly so. In the bed of the river it is pitted with 
numerous pot-holes a foot or soin diameter. The water averaged 
only about two feet deep on the shoals at the time of my visit,. 
so that a pedestrian could pick his way across without much 
difficulty. It probably varies from less than half to more than 
twice that depth. It is always more or less turbid.. The dis- 


151 


charge of the river at this point varies from about 100 to 116,000 
cubic feet a second, and averages about 6,700. As a rule the 
maximum occurs in March and the minimum in September. 

The rocky bottom projects above the water in many places, 
and in some of the quieter spots there are deposits of sand and 
silt; so there is naturally some local diversity in the vegetation. 
In the following list, however, all the plants found growing in 
the channel of the river at the shoals are included. They are 
divided into trees, shrubs and herbs, and those in each group 
arranged as nearly as possible in order of abundance. The trees 
are all rather stunted, as might be expected. 


TREES HERBS 
Platanus occidentalis L. Panicum virgatum L. 
Betula nigra L. Hymenocallis coronaria (LeConte) Kunth. 
Liquidambar Styracifiua L. Dianthera Americana L. 
Salix nigra Marsh. Scirpus Americanus Pers. é 
SHRUBS Zizaniopsis miliacea (Mx.) Doell. & Asch. © 
Alnus rugosa (DuRoi) Koch Osmunda regalis L. 
Cephalanthus occidentalis L. Triadenum petiolatum (Walt.) Raf. 
Hypericum galioides Lam. Harperella fluviatilis Rose. 
Ttea Virginica L. Eleocharis mutata (L.) R. & S. 


The occurrence of a Podostemon in such a place would not have 
been at all surprising, but it was not detected. 

Most of the species listed are rather common and widely 
distributed, but three or four of them are here some distance 
from the localities given for them in Mohr’s Plant Life of Ala- 
bama, and two or three deserve special mention. 

The Hymenocallis, although perhaps not quite the most abun- 
dant herb, was the most conspicuous element of the vegetation 
at the time, being in full bloom. From a distance its numerous 
large white flowers gave somewhat the appearance of a thin layer 
of snow. Up to 1go1 this species seems to have been reported 
only from rocky shoals in muddy rivers just above the fall-line 
near Columbia, S. C., and Augusta, Ga. In the year named Dr. 
Mohr (in his Plant Life of Alabama, p. 447) added a third station, 
very similar to the others, namely, the Warrior River near Tusca- 
loosa, where it was found by Dr. Eugene A. Smith. That locality 
having been drowned out several years ago, Squaw Shoals is 


152 


now the lowest possible station.for the plant on that river. But 
about the same time that I visited Squaw Shoals Mr. R. S. Hodges 
of the Geological Survey of Alabama saw what is undoubtedly 
the same species in similar situations in a creek near Helena, 
She by County, where it seems to be in no immediate danger of 
extermination. 

Strange to say, this rare and handsome plant is not mentioned 


Fic. 2. View of Squaw Shoals looking diagonally up-stream from site of lock on 
left bank. 


in either edition of Small’s Flora of the Southeastern States, even 
as a synonym. Although it might be difficult to distinguish 
from H. occidentalis in the herbarium, it differs greatly from that 
species in habitat, and blooms about two months earlier; approxi- 
mately at the same time as an unidentified Hymenocallis in 
South Georgia of which I published a photograph a few years 
ago.* 

It seems rather strange to find a plant with a large bulb and 
succulent leaves growing in running water, but this probably 
indicates that the rocks to which it is attached are often exposed 
to sun and wind for a few weeks in the fall, when the water is 
lowest. 


* Bull. Torrey Club 32: 463-465. f. 5. ro05; Ann. N. Y. Acad. Sci. 17: 257. 
pl. 24. 1906. 


153 


The Harperella is even less known to botanists than the 
Hymenocallis, having been found previously only in rocky beds 
of streams on Sand and Lookout Mountains in northeastern 
Alabama, and that only since 1905.* It was not in flower or 
fruit at the time, and I did not collect specimens, so that this 
new locality may never be represented by evidence of the kind 
demanded by some systematists. 

Eleocharis mutata is another comparatively rare species, pre- 


Fic, 3. Hymenocallis coronaria at Squaw Shoals, in about a foot of water. 


viously reported in the United States only from the glaciated 
region and coastal plain, where it grows usually in ponds.t 

On the loamy banks of the river at this place are found among 
other things Alnus rugosa, Kalmia latifolia, and Batodendron 
-arboreum, which cannot endure much fluctuation of water, and 
Fraxinus caroliniana and Breweria humistrata, which are chiefly 
confined to the coastal plain. 

It is one of the ironies of fate that the shoals, rapids and falls, 


* See Torreya 6: 112-114. 1906; 10: 237-239. 1910. The plant was then 
referred to H. nodosa, H. fluviatilis not having been described until afterward. For 
description of the latter see Rose, Contr. U. S. Nat. Herb. 13: 290. 1911; Small, 
Sab Os Ss ed 213555 sore. 

7 See Mohr’s Plant Life of Ala. 396-397; also Rhodora 7: 72. 1905. 


154 


which are in many ways the most interesting spots on our rivers, 
are the very places that are doomed to obliteration first by the 
commercialistic ‘‘development’’ of water-power or navigation, 
or both—as is planned at Squaw Shoals. The controversy over 
Niagara Falls is of course familiar to all; and there are other in- 
stances of the same sort of work in progress in Alabama. At this 
very time one of the water-power syndicates is threatening to 
build a dam across Little River at the lower falls on Lookout 
_Mountain, a spot noted for the occurrence of such rare plants 
'as Rhododendron catawbiense, Chondrophora virgata, Harperella 


Fic. 4. Fatch of Panicum virgatum and Dianthera americana on Squaw Shoals, 
with small trees at left. 


fluviatilis, the mountain form of Sarracenia flava, and several 
species chiefly confined to the coastal plain.* 

The greatest loss to science in such cases is not the mutilation 
of the scenery (the chief contention at Niagara), nor even the 
destruction of stations for the rare plants, for the same species 

* See Torreya 6: I14. 1906. 


155 


can still be found elsewhere. It is the termination of the oppor- 
tunity to study various interesting problems of potamology and 
phytogeography,* as for example, how so many coastal plain 
plants managed to establish themselves or persist in these interior 
localities. As no two shoals are exactly alike, the effacement of 
any one of them is an irreparable loss. But as it is impossible 
to measure such a loss in money, there is not much hope that the 
interests of science will ever be permitted to outweigh those of 
commercialism. ; 


A NEW NORTHEASTERN SEDGE 


By KENNETH K. MACKENZIE 


In addition to several species, which are also of wide European 
distribution, the group of which Carex flava L. is best known, is 
represented in the northeastern part of North America by a 
widely distributed plant which is unlike anything known from 
Europe. In all the European species of the group characterized 
by long beaked perigynia, the perigynia beaks are rough and 
strongly brownish-red tipped at the apex and the pistillate scales 
are also strongly brownish-red colored and very conspicuous in 
the spikes. In the American plant under discussion the perigynia 
beaks are smooth or obscurely few-toothed, under a microscope, 
and are whitish at the apex when young or in age are light 
tawny colored. The brownish-red tint is lacking in the scales, and 
the scales are very inconspicuous in the spikes, at maturity being 
concealed by the perigynia. These characters give this plant a 
markedly different appearance from that presented by the other 
members of this group, and enable it to be readily recognized 
in the field. 

This plant was long ago recognized as distinct from Carex 
flava L. by Dewey, who treated it as identical with the European 
Carex lepidocarpa Tausch. Olney distributed various specimens 


* See Bull. Torrey Club 32: 161. 1905; 37: I09. 1910; Geol. Surv. Ala. Monog. 
8: 148. 1913. Since the last publication appeared the dam of the Coosa River 
there referred to has been completed, flooding several square miles of country, 
including an unrecorded station for Sabal glabra, among other things. 


156 


of it as Carex flava L. and forma androgyna and forma lepidocarpa 
and remarked that the forms with a nearly sessile staminate spike 
and the forms with a strongly peduncled staminate spike were 
often found in the same clump (Olney Car. Bor.-Am. 7). Bailey 
treated the plant as Carex flava var. graminis Bailey, but prob- 
ably included other elements in his conception of his variety, 
especially the plant covered by his reference to the rough beaked 
perigynia. The plant treated by Prof. Fernald as Carex flava 
var. rectirostra Gaudin is almost entirely the present species, 
as is also a portion of the plant he treats as Carex flava var. elatior 
Schlecht. The description of the plant called Carex lepidocarpa 
Tausch by me in Britton & Brown’s Illustrated Flora (2d ed.) 
is also taken from the present species. 

When the really distinguishing features of this plant are, how- 
ever, understood, it is readily told from all its allies and should 
no longer be confused with any of them. 

Carex flava, itself, is further distinguished by the noticeably 
longer perigynia (5-6 mm. long), the leaf-blades averaging wider 
(2-5 mm. wide), the sharper culms and more yellowish aspect of 
the whole plant. The tendency of the pistillate spikes to be 
staminate at the top is also much less developed. 

In North America genuine Carex lepidocarpa seems to be con- 
fined to the extreme northeastern part. I have seen specimens 
only from the Gaspi region and from St. Pierre. The extremely 
long-peduncled staminate spike usually serves as an additional 
means to distinguish this species. 

What I take to be the plant described from Maine by Kiiken- 
thal (Pflanzenreich IV: 673) as var. laxior of Carex lepidocarpa 
Tausch is more closely allied, but in addition to the points 
already discussed can be distinguished by its sharp-angled culms 
and green shorter-beaked perigynia. The beaks of the perigynia 
in this plant are exceptionally rough. 

I have seen numerous specimens of this species Sere show 
that it ranges from Maine and Quebec as far West as Indiana 
and Wisconsin. In New Jersey, where I have become well 
acquainted with it, it is confined to the northwestern counties 
where it occurs in wet calcareous meadows, in which situation 


157 


it is often locally common. My number 4645 collected at 
White Pond, Sussex County, near Andover Junction, on June 26, 
1910, may be designated as the type. 

The species may be described and known as: 


ea Carex cryptolepis sp. nov. 
“ Carex lepidocarpa Tausch,”’ Dewey, Wood’s Class Book (2 Ed.). 
585. 1847. 
Carex flava L. var. graminis Bailey, Mem. Torr. Club 1: 30 (in 
part). 1887. 


“ Carex flava L. var. rectirostra Gaud.”’ Fernald Rhodora, 8: 211 
(in part). 1906. 

“Carex flava L. var. elatior Schlecht.’’ Fernald 1. c. (in part). 
1906. 

“Carex lepidocarpa Tausch,’’ Mackenzie in Brit. & Brown III. 
Flora (2d ed.): 430 and fig. 1076. 1913. 


Densely cespitose, not stoloniferous, the culms erect, slender. 
2-6 dm. high, smooth or very nearly so, obtusely triangular below, 
acutely triangular above, phyllopodic, light brown at base, 
exceeding culm leaves, but mostly exceeded by leaves of sterile 
shoots. Leaves 4-6 to a fertile culm, on lower fourth, but not 
bunched, light green, the blades erect, flat, 1.5-3 mm. wide, 
usually 0.5-2.5 dm. long, roughened towards apex, not strongly 
septate, the sheaths conspicuously white-hyaline ventrally, not 
prolonged upwards at mouth; sterile shoots phyllopodic, con- 
spicuous, the blades averaging longer. Staminate spike subses- 
sile to strongly peduncled, 7-18 mm. long, 2-3 mm. wide, occa- 
sionally partly pistillate at base, its scales oblong-lanceolate, 
greenish-yellow with green midvein, acute. Pistillate spikes 3 
or 4, the upper one or two approximate, the next strongly sepa- 
rated and the lowest often very strongly separated, mostly 
staminate at apex, sessile or lower exsert-peduncled, oblong, Io- 
20 mm. long, 7-10 mm. wide, closely 15-35 flowered in many 
ranks, the upper perigynia ascending, the middle spreading and 
the lower reflexed; bracts leaf-like, sheathing, the lower with 
erect, the upper with widely spreading blades. Scales lanceolate, 
acute, greenish-yellow with green midvein, narrower than and 
about length of body of perigynia, concealed and_inconspicuous 
at maturity. Perigynia light- or yellowish-green, or at maturity 
yellowish, 4-4.5 mm. long, the body obovoid, 1.75 mm. wide, 
inflated, suborbicular in cross-section, the upper part empty, 


158 


coarsely about Io-nerved, round-tapering to a sessile base, 
abruptly slender beaked, the beak nearly as long as body, straight 
or the lower bent, smooth or very obscurely few toothed, promi- 
nently bidentate, the teeth smooth, closely contiguous to one 
another, whitish or in age light tawny tinged. Achenes obovoid, 
triangular, 1.5 mm. long, I mm. wide, blackish, slightly silvery 
shining, prominently pitted, apiculate, jointed with slender, bent, 
at length deciduous style. Stigmas three. 


SPECIMENS EXAMINED 


QuEBEC. Notre Dame du Lac, Northrop 202; Aug. 13, 1887 
(C); Lake Edward, Brainerd, Aug. 1, 1901, and Aug. 21, 1896 (B). 

Maine. Mt. Desert Island, White, Sept. 5, 1891 (C); Moose- 
head Lake, C. E. Smith (C); Great Pond, Mt. Desert Island, 
Rand, June 23, 1892 (C). 

VERMONT. Stratton, Brainerd (B) and also Grout, July 4, 
1895 (C); East Wallingford, Eggleston 1684, July 11, 1899 (N. Y.); 
Newfane, Howe, Aug. 1, 1891 (N. Y.); Lake Dunmore, Braimerd, 
July 11 and Aug. 11, 1896 (B); East Middlebury, Braznerd, 
July 12, 1890 (B); Sudbury, Brainerd, Aug. 14, 1896 (B); 
Enosburgh, Brainerd, July 17, 1895 (B). 

Mass. Essex Co., Oakes (N. Y.); Needham, Forbes, July 18, 
1902 (K. M.). 

RHODE IsLAND. Providence, Olney, marked “C. lepidocarpa 
Dewey! Tausch? not of Kunze!” (C); Cumberland and East 
Providence, Olney, July 22 and 26, 1871 (C& N. Y. & K. M.); 
Thurber 1846 (N. Y.). 

NEw York. Lake Mohegan, Leggett, July 9, 1868 (C); 
Pyramid Lake, Britton, Sept. 2, 1900 (N. Y.); Whitesboro, 
Haberer, June 1883 in part (N. Y.); Adirondack Mts., E. C. 
Howe, July (N. Y.); Paradox Lake, Brainerd, Sept. 9, 1882 (B). 

NEw JERSEY. Waterloo, Britton and Porter, July 28, 1885 (C); 
Stanhope, Morris Co., Mackenzie 2118, June 24, 1906 (K. M.); 
White Pond, Sussex Co., Mackenzie 826, July 31, 1904 (K. M.); 
Andover Junction, Sussex Co., Mackenzie 4671, July 26, 1910 
(K. M.). 

OnTARIO. Sarnia, Lambton Co., Dodge, Aug. 1, Ig11 (K. M.); 

e Victoria, Brainerd, Sept. 13, 1901 (B). 


, 159 


MicHIcAN. Grand Rapids, Miss Cole, June 8, 1892 (K. M.); 
Harsen’s Island, St. Clair County, Dodge, July 18, 1911 (K. M.); 
Port Huron, St. Clair County, Dodge, July 17, 1911 (K. M.). 

INDIANA. Grass Lake, Steuben Co., Deam 1202, July 22, 1906 
{N. Y. & K. M.); Wolf Lake, Mrs. Chase 1396, July 26, 1900 
{K. M.). 

WIsconsIN. Milwaukee, Hasse, June 25, 1882 (N. Y.). 


— 


= 


ADDITIONS TO THE PLEISTOCENE FLORA OF: THE 
SOUTHERN STATES* 


By EDWARD WILBER BERRY 


During the last few years I have collected or received for 
identification several small collections of fossil plants from various 
localities and horizons in the Pleistocene of North Carolina, Ala- 
bama and Mississippi, and since these should be a matter of 
published record for the benefit of botanists and others interested 
in the question of the former distribution of existing species, the 
following brief compilation has been made. 


NortTH CAROLINA 


The first of these collections is from North Carolina. A most 
interesting deposit containing fossil plants was discovered in 
1906 on the right bank of the Neuse River about four and one- 
half miles above Seven Springs in Wayne County. The section 
shows at its base a tough blue clay interstratified with layers of 
leaves, fruits, wood, and other vegetable débris, overlain by 
sand and gravel, and exposed in the recent cutting of the river. 
‘The manner of occurrence indicates that at the time of deposi- 
tion the locality was at the head of a Pleistocene estuary, the 
plant material accumulating exactly as it is at the present time 
along the coastal plain rivers. The collection from this locality 
was of such exceptional interest that a short account of it was 
published in 1907.{ Thirty-eight species were listed, the locality 


* Published with the permission of the Director of the U. S. Geological Survey. 
- 7 The deposits are referred to the Chowan formation by Stephenson, N. C. Geol. 
Surv., 3: 285. 1913. ; 

ft Berry, E. W., Journ. Geol. 15: 338-340.. I907- 


160 


being referred to as Station 850. There remained a mass of 
fragmentary leaves and seeds. Some of the best preserved of 
the latter were subsequently submitted to the U. S. Biological 
Survey and were determined by Mr. W. L. McAtee. The large 
collection of recent fruits and seeds gathered together by the 
Biological Survey and the long experience of Mr. McAtee, in 
identifying the comparable remains found during extensive 
studies of the stomach contents of birds, renders these identifica- 
tions particularly authoritative. Following are the additions to 
this late Pleistocene flora: 

1. Chaetochloa sp. A caryopsis of a grass of the genus 
Chaetochloa Scribner. 

2. Sparganium sp. A nutlet of a bur-reed, specifically un- 
determinable. 

3. Populus cf. deltoides Marsh. The eae contain Sune 
dant bud-scales greatly resembling and probably those of this 
species, the leaves of which have been found in Pleistocene de- 
posits of very similar age in Alabama. 

4. Polygonum sp. An achene of an undetermined species of 
the genus Polygonum L. 

5. Viburnum cf. molle Michaux. Two stones, probably repre- 
senting this species, which is still found in this area. The present 
range of the species is from Massachusetts to Florida near the 
coast. 

6. Viburnum cf. nudum L. ‘Two stones, probably representing 
this species, whose present range is from Long Island to Florida. 

7. An achene of a species of Compositae resembling those of 
the genus Centaurea L. 

8. A single seeded dry drupe suggesting the family Oleaceae. 


FLORIDA 


In the vicinity of Milton, Santa Rosa County, Florida, there 
is a buried swamp deposit of late Pleistocene age containing 
trunks of a species of Pinus; and stumps, roots, and seeds of 
Taxodium distichum, as well as undeterminable fragments of 
dicotyledonous leaves.* 


* This deposit is mentioned in Harper, R. M., Peat deposits of Florida, pp. 295- 
297, 1910, and without any warrant is referred to the so-called Grand Gulf formation. 


161 


ALABAMA 


A few miles below Columbus, Georgia, along the west bank 
of the Chattahoochee River in Russell County and in the vicinity 
of Abercrombie Landing, the late Pleistocene terrace contains 
considerable deposits of impure peat which in places carries 
identifiable plant remains. A collection made here in 1907 by 
L. W. Stephenson was described by me that same year and twelve 
species were recorded.* I made additional collections in 1909 
and subsequently recorded four additional species. 

In a recent review of this material characteristic seeds of 
Phytolacca decandra L. were recognized, but since care was not 
taken to exclude recent seeds in the collecting of large specimens 
containing leaves, it is possible that this is a recent seed, although 
it has the appearance of being fossil and not recent. In addition 
to the foregoing the stones of an undetermined species of Rubus 
were identified from this locality. 

During 1913 Dr. C. W. Cooke of the U. S. Geological Survey 
made a collection of leaves from a grey argillaceous sand exposed 
about three miles west of Monroeville, Monroe County. The 
elevation is about 470 feet and the material is of a sort which is 
characteristic of what has hitherto been called Lafayette forma- 
tion in this region. The collection, while not large, contains the 
following forms: 


Arundinaria sp. (probably Quercus virginiana Miller 
macrosperma Michx.) Platanus sp. (probably occi- 
Hicoria aquatica (Michx. f.) dentalis L.) 
Britton Persea pubescens (Pursh) Sar- 
Quercus phellos L. gent 


These six forms are all still existing and all of them have pre- 
viously been recorded from the Pleistocene of the southern coastal 
plain so that I have no hesitation in asserting that the deposits 
are of Pleistocene age. 

MISSISSIPPI 

In 1910 I collected the following plants from a clay-lens in the 

Pleistocene terrace materials exposed along the Chickasawhay 


* Berry, E. W., Amer. Nat. 41: 689-697. pl. I-2. 1907. 
7 Berry, E. W., Amer. Jour. Sci. iv. 29: 387-398. I9I0. 


162 


River, one and one-half miles above Chicoria in Wayne County: 


Taxodium distichum (L.) L. C. Betula nigra L. (leaves) 

-- Rich. (cone) Quercus phellos L. (leaves) , 
About ten or twelve miles up the river from this locality, C. W: 

Cooke made a small collection of fossil leaves in 1913. The 

locality is on the Chickasawhay River four miles northwest of 

Waynesboro in Wayne County. This collection contains identi- 

fiable leaves of the following species: 

Hicoria aquatica (Michx. 3) Quercus predigitata Berry 
Britton Fagus americana Sweet 


Quercus phellos L. ; 
All of these are forms that are of widespread occurrence in the 
late Pleistocene of southeastern North America. 


JOHNS HOPKINS UNIVERSITY, 
BALTIMORE, Mp. 


SHORTER NODES 


OccURRENCE OF INDIAN PipE.—The article of Mr. Edwin 
D. Hull in the June number of TorreEya on the “Occur- 
rence of the Indian Pipe (Monotropa uniflora) in a Xero- 
phytic Habitat’ reminds me that in 1911 the plant was 
fairly abundant in a swamp of mingled black spruce and 
tamarack, the former predominating, in northwestern Wisconsin 
(Gaslyn, Burnett County). The individuals were somewhat 
dwarfed and blackened and were mostly concealed by the 
Sphagnum. They were in flower about the first of August. 
I had not visited the locality before nor have I since, but it im- 
pressed me as being a permanent habitat of these plants which I 
do not recall having seen elsewhere in the vicinity. : 

J.J? DAviche 
“ MODERN”’ BOTANY IN 1821 
» INE Cuntosa 
“Alte Zeit und neue Zeit. 


““FRAGER: Was ist Botanik? 
“LINNAEUS: Est scientia naturalis, quae vegetabilium. cogni- 
tionem tradit. (Philos. bot. 1. 1750.) 


163 


“Das JAHR 1821: Botanik ist die photoskotochromo?thermokry- 
ohydrogeoaérooryktozoophytoanthropobiomor phostoechiogeni- 
metriskopische Phytologie.’”’ (From Flora 5: 224. 14 Ap 1822.) 


PROCEEDINGS OF THE CLUB 
APRIL 14, 1914 

The meeting of April 14, 1914, was held at the American 
Museum of Natural History at 8:15 P.M. President Harper 
presided. Seventy-nine persons were present. 

The announced scientific program consisted of an illustrated 
lecture on ‘‘Edible Fungi,” by Dr. W. A. Murrill. This lecture 
will be published in full in the Journal of the New York Botanical 
Garden. 


- Adjournment followed. 
MiIcHAEL LEVINE, Sec. protem 


APRIL 29, 1914 

The meeting of April 29, 1914, was held in the Laboratory 
of the New York Botanical Garden at 3:30 P.M. President 
Harper presided. Eighteen persons were present. 

The minutes of the meeting of April 14 were read and approved. 

The committee appointed to draw up resolutions on the 
death of Dr. C. B. Robinson presented the following resolutions: 

WHEREAS, The members of the Torrey Botanical Club have 
learned with the deepest sorrow of the death of their fellow- 
member, Dr. Charles Budd Robinson, at the hands of certain 
barbarous residents of Amboina Island in the Dutch East 
Indies, be it therefore 

Resolved, That the Torrey Botanical Club desires hereby to 
place on record its appreciation of the accurate, scholarly char- 
acter of the scientific work accomplished by Doctor Robinson, 
its admiration of his boundless industry and of his frank and 
loyal personality, and its profound regret that a career of such 
substantial achievement and abundant promise should have been 
brought to so untimely an end, and 
_ Resolved, That these resolutions be entered upon the minutes 
of the Club and that a copy be transmitted to his family. 


164 


These resolutions were adopted. 

A communication from Edward F. Bigelow, Presiderit of the 
Agassiz Association, in which the Torrey Club is invited to make 
a field excursion to Arcadia, Sound Beach, was read and referred 
to the chairman of the field committee with power. 

The resignation of Miss Helen Palliser was read and accepted. 

Mr. Edward Nelson, Agricultural Experiment Station, Gaines- 
ville, Florida, was elected to membership. 

The first number on the announced scientific program consisted 
of a brief paper on ‘‘Observations on Sphaersoma and allied 
genera,” by Dr. Fred J. Seaver. This paper will be published 
in full in Mycologia for May. 

The second paper was given by Dr. N. L. Britton, on “The 
vegetation of the smaller islands belonging to Porto Rico.” Dr. 
Britton exhibited a number of specimens and photographs of 
plants collected on the islands of Desechao and Mona. Lists of 
the plants found on these islands will be compiled for future 
publication. 


Adjournment followed. 
B. O. DODGE, 


Secretary 
MAY 12, 1914 
The meeting for May 12, 1914, was held at the American 
Museum of Natural History with President Harper presiding. 
Seventy-five persons were present. 
The announced scientific paver consisted of an ithaca 
lecture on ‘‘Wild flowers of spring,’’ by Dr. N. L. Britton. 


Adjournment followed. 
B. O. DODGE, 


Secretary 
MAy 27, 1914 

The meeting of May 27, 1914, was held in the Laboratory of 
the New York Botanical Garden at 3:30 P.M. with Vice-president 
Barnhart presiding. Ten persons were present. 

The minutes of the meetings of April 29 and May 12 were read 
and approved. 

Mr. G. A. Reichling, Brooklyn, N. Y., was elected to member- 
ship. 


165 


The first number on the scientific program consisted of a paper 
on “Some midwinter algae of Long Island Sound,” by Dr. 
Marshall A. Howe. The paper will be published in full in June 
TORREYA. . 

The second paper was presented by Dr. Michael Levine on 
“The origin and development of lamellae in Coprinus micaceus.”’ 


Adjournment followed. 
Be Of; DODGE: 


Secretary 
NEWS ITEMS 


The board of trustees and the director of the Missouri Botanical 
' Garden have issued invitations to the celebration of the twenty- 
fifth anniversary of the organization of the garden, to be held in 
St. Louis, October fifteenth and sixteenth. Addresses will be 
made by the director, Dr. G. T. Moore, and by many visiting 
botanists. Some of the foreign speakers, who include professors 
Wille, Lipsky, Briquet, Czapek, Fitting and Klebs, may have 
difficulty in reaching St. Louis on account of the war, but “‘it is 
known that all of those on the program will make every effort 
to come.”’ The celebration will not be postponed. Besides the 
speeches the celebration includes inspection of the buildings 
and grounds, a motor trip through the city, and a dinner by the 
trustees to invited guests at the Liederkranz Club. 


Professor Guy West Wilson, who during the past year has 
been employed by the Federal Government as an agent of 
the laboratory of forest pathology in the investigation of the 
chestnut bark disease in cooperation with Dr. Mel T. Cook 
of the New Jersey Experiment Station, has been appointed to 
the newly created chair of mycology and plant pathology in 
the State University of Iowa at Iowa City, Iowa, with the rank 
of assistant professor. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six 
gratuitous copies of the number of TorReYA in which their papers 
appear, will kindly notify the editor when returning proof. 

; Reprints should be ordered, when galley proof is returned 
to the editor. The New Era Printing Co., 41 North Queen 
Street, Lancaster, Pa., have furnished the following rates: 


2pp 4pp 8pp 12pp 16pp 20pp 
25 copies $ .75 $1.05 $1.30 $1.80 $2.20 $2.50 
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200 copies 1.70. 2.35 2.90 3.75 4.35 4.70 
Covers: 25 for 75 cents, additional covers 1 cent each. 
Plates for reprints, 40 cents each per 100. 


The following Committees have been appointed for 1914 


Finance Committee Field Committee 
4 dsb: BaRNHART, Chairuian © SERENO STETSON, Chairman 
Miss C. C. Haynes 
Budget Committee Program Committee 
J. H. Barnuart, Chairman Mrs. E. G. Britton, Chairman 
N. L. Britron Miss JEAN BROADHURST 
B. O. DopGE C. SruaRT GAGER 
M. A. Hower F. J. SEAVER 
A. W-. Evans 
H. H. Ruspy 


Local Flora Committee 
N. L. Britron, Chairman 


Phanerogams: - Cryptogams: 
E. P. BicKNELL Mrs. E. G. Brirron 
N. L. Brirron Puitip DowELL 
CGy Curtis Tracy E. Hazen 
~K. Ko. Mackenzie > - - M. A. Howe 
_ Norman Tayior W. A. Murrite 


Delegate to. the Council of the New York Academy of Sciences 
WILLIAM MANSFIELD 


OTHER PUBLICATIONS 


OF THE 


TORREY BOTANICAL CLUB 


(1) BULLETIN 


A monthly journal devoted to general botany, established 
1870. — Vol. 40 published in 1913, contained 712 pages of text — 
and 26 full-page plates. Price $3.00 per annum. For Europe, 
14. shillings. Dulau &. Co., 37. Soho Square, London, are, 
agents for. England. ee 

Of former volumes, only 24-40 can | be supplied entire ; cer- 
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of some numbers has been reserved for the completion of sets. 
Vols. 24-27-are furnished at the published price of two dollars 
each; Vols. 28-40 three dollars each. 

Sinele copies (30 cents) will be furnished only when not 
breaking complete volumes. 


(2) MEMOIRS 
The Memoirs, established 1889, are published at irregulas 
intervals. Volumes 1-13 are now completed ; Nos. 1 and 2 of 
Vol. 14 have been issued. The subscription price is fixed at 
$3.00 per volume in advance. The numbers can also be pur- 
chased singly. A list of titles. of the individual papers and of 
‘prices will be furnished on application. 


(3) The Preliminary Catalogue of Anthophyta and Pteri- 
dophyta reported as growing within one hundred miles of New 
York, 1888. Price, $1.00. 


Correspondence relating to. the above publications should be 
addressed to : 
DR. BERNARD O. DODGE 
Columbia University 
| New York City 


‘Vol. 14 October, IQI4 No. I0 


ORREYA _ 


A Monruty JourNnat or BoranicaL NoTes anp News 
EDITED FOR 


THE TORREY BOTANICAL CLUB 


BY 


NORMAN TAYLOR 


JOHN TORREY, 1796-2873 


CONTENTS 
The Vegetation of Connecticut. III. Plant societies on uplands: G. E Nicos 167. 
Algal stalactites in Bermuda: J. W. HARSHBERGER..,....00.....0scsecesee cdees crseenorens 195 
On Erigeron pusillus Nutt.: N. L. BRITTON 2.005002. 20cceenseces veseav ete cris tv cvaty-cepeseee 197 


News Items... ..... NS AA IMIG Bp ORE OES Nk SNP PRP NN Bchc eden ecocnt ee oonec eras 199 


PUBLISHED FOR THE CLUB 


At 41 NortH Quzen Street, LaANcAstzER, Pa. 
BY THe New Era Printinc COMPANY 


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THE TORREY BOTANICAL CLUB 


OFFICERS FOR 1014 


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R. A. HARPER, Pu.D. 


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JOHN HENDLEY BARNHART, A.M., M.D. 
HERBERT M. RICHARDS, S.D. 


Secretary and Treasurer 
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Columbia University, New York City 


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ERNEST D. CLARK, Px.D. HERBERT. M. RICHARDS, S.D. ; 
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NORMAN TAYLOR 


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TORREYA 


October, Ig14. 
Vol. 14 No. Io 


THE VEGETATION OF CONNECTICUT 


III. PLANT SOCIETIES ON UPLANDS* 


By GEORGE E. NICHOLS 


In the first paper of this series the writer undertook to point 
out and in a measure to account for certain of the broader features 
of the vegetation of Connecticut. In the second an account 
is given of the virgin forests. In the present and subsequent 
papers attention will be devoted primarily to the study of plant 
societies and their relationship both to one another and to 
environment. Numerous writers during the past few years have 
dealt with this phase of vegetation in other parts of the country, 
but so far as published records show very little work of this 
nature seems to have been accomplished in southern New England. 
Since it is desired that this series of studies may serve as a starting- 
point for further investigations, both extensive and intensive, it 
has seemed advisable to treat the subject matter more or less 
comprehensively, drawing freely upon the observations of other 
workers in the same field of study. 

The scheme of classification which in a general way underlies 
the writer’s treatment of the plant societies of Connecticut is 
the one originated some years ago by Cowles.f This classi- 
fication ‘attempts to relate plant societies not only to water, but 
also to soil, and more especially to the physiography.’’ The 
fundamental concept of the scheme is that “‘each particular 

* Contribution from the Osborn Botanical Laboratory. 

+ Cowles, H. C. The physiographic ecology of Chicago and vicinity. Bot. 
Gaz. 31: 73-108, 145-182. f. I-35. 1901. Reprinted with slight modifications 
as Bull. Geog. Soc. Chicago No. 2. Igot. 

[No. 9, Vol. 14, of TORREYA, comprising pp. 149-166 was issued 18 September 
1914.] 

167 


Li 

NB} 
801 

GA 


168 


topographic form has its own peculiar vegetation. This is due 
to the fact that the soil conditions upon which plants depend are 
determined by the surface geology and topography.’”’ And, 
since the nature of the topography is constantly undergoing 
modifications as a result of erosion and deposition, it follows 
that ‘“‘just as there is an order of succession of topographic forms 
in the changing landscape,” so ‘“‘there must be an order of suc- 
cession of plant societies. As the years pass by, one plant society 
must necessarily be supplanted by another, though the one passes 
into the other by imperceptible gradations.’’ Such a classifi- 
cation, it will be seen, is at once genetic and dynamic. It aims 
to “group plant societies according to their relationship and 
their evolution.”’ | 

In a more recent contribution Cowles* has defined three types 
of vegetative succession, regional, topographic, and _ biotic. 
Regional successions are due primarily to secular changes in 
climate and move with extreme slowness. In Connecticut the 
series of changes in vegetation that have ensued since the retreat 
of the continental ice sheet serve to illustrate this type of suc- 
cession. Topographic successions “‘are associated with the 
topographic changes which result from the activities of such 
agencies as running water, wind, ice, gravity, and vulcanism.”’ 
Such successions in Connecticut are seen principally along rivers 
and along the coast. Topographic successions take place much 
more rapidly than regional successions. Biotic successions are 
instituted by plant and animal agencies. On account of the 
comparative rapidity with which these agencies operate and their 
far-reaching influence, this type of succession must be regarded 
as more important than either of the two preceding. “If, in 
their operation, regional agencies are matters of eons, and topo- 
graphic agencies matters of centuries, biotic agencies may be 
expressed in terms of decades.” 

In treating the plant societies of Connecticut and their eco- 
logical relations, it has been found convenient to group them in 
the following manner.* 

* Cowles, H. C. The causes of vegetative cycles. Bot. Gaz. 51: 161-183. 


IQII. : 
7 Compare Cowles, 1901, op. cit. 


169 


Plant societies on uplands. 

Plant societies in lowlands. 

Plant societies along rivers and streams. 

. Plant societies along the coast. 

Broadly ne the term lowland is here used to designate 
depressions of all sorts—areas ‘occupied by lakes, swamps, etc. 
All other types of topography are included under uplands. In 
the present paper attention is confined to upland successions. 


B&O NH 


By way of introduction a representative upland succession, such 
as may be studied along the trap ridges in the vicinity of New 
Haven, will be described. Then, with this as a background, 
differences between successions on various substrata and in 
different parts of the state will be considered. | 

Probably nowhere in this region are the environmental con- 
ditions to which vegetation is subjected more severe than on the 
bare surface of an exposed rock. Insolation during the daytime 
is intense, temperature changes are extreme, and water is absent 
for long periods. Add to these the difficulty, where the surface 
slopes and crevices are absent, of securing a foothold, and it is 
evident that even among xerophytes comparatively few plants 
are qualified to exist in such localities. Usually the first living 
organisms to appear on a freshly exposed trap surface are crustose 
lichens, e. g., Buellia petraea and Lecanora cinerea. These form 
a black or grayish incrustation over the surface and adhere so 
tightly to the rock as to be practically inseparable from it. 
Immediately following these, but apparently dependent upon 
them for a foothold, frequently comes Physcia tribacea, a foli- 
aceous lichen whose rosette-shaped thallus for the most part 
is closely adnate to the substratum. These three plants repre- 
sent the pioneers of vegetation. Many crustose lichens are 
said to secrete acids by means of which they effect to a certain 
extent the disintegration of the rock on whose surface they 
occur. In this way, as well as by their very presence, they tend 
to create a substratum upon which it becomes possible for foliose 
and fruticose lichens and certain mosses to secure a foothold. 
And not only do the crustose lichens prepare the way for other 
plants, but by so doing they pave the way for their own de- 


170 


struction; for with the advent of taller, shade-producing forms 
they are speedily eliminated. There may be three more or less 
distinct lichen sub-stages, viz., crustose, foliose, and fruticose; 
but as a rule the last two are more or less completely telescoped 
into one. Of the foliose lichens the most conspicuous in the 
trap-rock succession is Parmelia conspersa, a form which often is 
so abundant as to almost obscure the rock surface over consider- 
able areas. But sometimes other foliose species are equally 
important, notably Dermatocarpon miniatum, Umbilicaria penn- 
sylvanica, and Parmelia caperata; while not infrequently Ste- 
veocaulon paschale, one of the most characteristic of the fruticose 
lichens along the trap ridges, usurps the soil prepared by the 
crustose lichens. Associated with these lichens, and equally 
capable of thriving wherever they can secure foothold, are a few 
mosses, é. g., Grimmia Olneyi and Hedwigia ciliata. 

The rapidity with which not only the changes just described, 
but subsequent changes as well, are brought about is influenced 
of course to a greater or less extent by the nature of the site—the 
degree of exposure to sun and wind, steepness of the rock surface, 
etc. Succession almost invariably proceeds more rapidly along 
the lower slopes of a hill than near its crest, due to the lesser 
exposure here. The relative abundance of seepage water as 
the bottom of a hill is approached, also furthers rapid succession. 

Thus far observations have been restricted to the vegetation of 
the rock face. Attention must now be directed to another phase 
of the trap rock succession, viz., succession. in the crevices. 
Crevices due to various causes are found in greater or less abun- 
dance in practically all exposed rocks. ‘Trap rocks especially, on 
account of the peculiar manner in which they were formed, are 
characterized by the presence of numerous fissures. In these 
fissures, and in hollows of the rock surface, dust and sand collect, 
thus favoring the conservation of moisture and making it possible 
for plants to develop whose roots or rhizoids require a soil. The 
pioneer crevice plants are fruticose lichens and mosses. Of the 
lichens, the majority belong to the genus Cladonza, e. g., C. rangi- 
ferina, C. uncialis, C. furcata, C. sylvatica, C. pyxidata. Of the 
mosses, Ceratodon purpureus, species of Polytrichum (P. commune, 


17a 


P. piliferum, P. juniperinum), Leucobryum glaucum, and Dicra- 
num scoparium are prominent. Closely following these, and 
indeed often contemporaneous with them are certain Pterido- 
phytes and the advance guard of the Angiosperms—the group 
which ultimately is destined to predominate. The appended 
list includes a few of the more conspicuous herbaceous vascular 
plants characteristic of crevices in trap. 


Selaginella rupestris Danthonia spicata 
Woodsta tlvensis Krigia virginica 
Andropogon scoparius Lechea tenutfolia 
Aquilegia canadensis Opuntia vulgaris 
Aristida dichotoma Poa compressa 
Campanula rotundifolia Potentilla argentea 
Corydalis sempervirens Rumex Acetosella 


Saxifraga virginiensis 
It will be noted that most of the species here mentioned are 
perennial, and necessarily all are xerophytes. 

Notwithstanding that crevice plants and rock face forms are 
contemporaneous, the crevice vegetation, for the sake of con- 
venience, may be regarded as the second stage in the succession 
on trap (fig. 1). Onsteep slopes this condition may be protracted 
indefinitely. But as a rule a third stage is soon inaugurated by 
the encroachment of the crevice vegetation on neighboring 
portions of the rock face; and where, as on gentle slopes, the soil 
collects not only in crevices but in shallow depressions of any 
sort, the surface of the rock may soon become clothed with a 
more or less continuous plant cover. The spreading out of the 
crevice colonies is accelerated by the continued accumulation 
alongside of windblown particles of inorganic matter and frag- 
ments of vegetable debris. It is hardly necessary to more than 
suggest the improved condition of the rock as a habitat for 
plants which results from the development of a soil. The usual 
pioneers on such an area are the lichen and moss species already 
present in the crevices, and it is a common occurrence to find 
flat rocks and gentle slopes completely overgrown by loose masses 
of Cladonia, thin mats of Ceratodon, or dense colonies of Poly- 
trichum. But the prestige of these lower forms is short lived, 


172 


for as soon as sufficient soil has accumulated they are superseded 
by grasses and other vascular plants. These, by means of their 
interlacing roots and rhizomes bind the soil together more firmly, 
and in this way a sod is gradually developed. Because of their 
omnipresence and the abundance of their tough, fibrous roots, 
the bunch grass (Andropogon scoparius) and the wire grass (Poa 
compressa) are especially important as sod formers. The wire 


Fic. 1. Rock face and crevice vegetation on trap; near summit of West Reck, 


New Haven. The conspicuous lichen in the foreground is Parmelia conspersa. 
Among the crevice forms are Leucotryum glaucum and other mosses, Cladonia sp.» 
Woodsia ilvensis, Andropogon scoparius, and Rhus typkina. The tree in the 
background is Juniperus virginiana. 


grass possesses an additional advantage in that it develops long 
rhizomes which facilitate the invasion of new territory. There 
may thus arise a plant society characterized by the prevalence 
of tall, perennial grasses. Associated with the two grasses already 
mentioned may occur many other herbaceous plants, some of 
which are here noted. 


173 


Antennaria plantaginifolia Lespedeza Nuttallir 

Aster linaritfolius Liatris scariosa 

Aster patens Poa pratensis 

Carex pennsylvanica Pteris aquilina 

Cerastium arvense Pycnanthemum virginianum 
Comandra umbellata Sericocarpus asteroides 
Helianthus divaricatus Solidago nemoralis 
Lespedeza capitata Viola pedata 


Up to this point in the succession herbaceous: plants have pre- 
dominated. But some shrubs usually appear in the crevice 
stage (fig. 1) and by the time the rock has become sod-covered 
they may have increased in number to such a degree as to become 
the controlling element of the vegetation. Very often it is 
possible to recognize a distinct shrub stage. Of the shrubs 
present at this time, a number may be cited as about equally 
characteristic, viz. 


Ceanothus americanus Rhus copallina 

Gaylussacia baccata Rhus glabra 

Myrica asplenifolia Rhus lirta 

Prunus virginiana Rosa humilis 

Quercus tlictfolia Vaccinium pennsylvanicum 
Quercus prinoides Vaccinium vacillans 


The next advance toward mesophytism is seen in the advent 
of trees. Like the shrubs, trees begin to appear early in the 
series, and their presence often exerts an appreciable effect on 
the character of the rock face and crevice vegetation. Poly- 
podium vulgare, for example, grows in crevices beneath the shelter 
of these scattered trees, but almost never out in the open. Many 
mosses are likewise restricted. Succession invariably is more 
rapid in the shade than in the open sunlight. Foremost in 
importance among the pioneer trees in the trap ridge succession 
near New Haven are the red cedar (Juniperus virginiana) and 
the post oak (Quercus steHata). The transition from the shrub 
stage to the pioneer tree stage is not abrupt, and, as a matter of 
fact, so simultaneously may the shrubs and trees make their 
appearance that quite as often as not the stages are telescoped 


174 


into one. Both the red cedar and the post oak require plenty of 
sunlight, 7. e., they are intolerant of shade. They never give 
rise to dense woodlands, but always form open, almost park-like 
groves (fig. 2). In the sunny patches between the trees the 
herbaceous and shrubby vegetation of the two preceding stages 
persists almost unaltered, but in shaded spots there begin to 
appear forms which are characteristic of the subsequent stage in 
the succession. 


Fic. 2. Pioneer tree stage along crest of West Rock ridge, New Haven. 


Between the scattered trees (Quercus stellata) occur patches of herbaceous vegeta- 
tion and shrubs. In the foreground is seen Helianthus divaricatus. The shrubs 
shown are Rhus typhina. 


Further significant changes in the physiognomy of the vege- 
tation are foreshadowed by the advent of such trees as the 
chestnut oak (Quercus Prinus) and the pignut (Carya glabra). 
These species, like the red cedar and post oak, are relatively 
xerophytic and on some accounts they should perhaps be classed 
with them as pioneer trees. But they differ in two im- 
portant respects, viz., they are slightly tolerant of shade, and 


175 


they attain a much larger size. Red cedars and post oaks more 
than thirty feet high are seldom encountered, but the pignut and 
chestnut oak commonly grow to a height of more than fifty feet. 
While, then, both the chestnut oak and pignut may put in their 
appearance early in the series, and while often they may be 
conspicuous members of the pioneer tree stage, their chief im- 
portance lies in the fact that as the trees grow larger they overtop 
the cedar and post oak; and as they become more numerous, 
their crowns forming a more or less continuous canopy, the red 
cedar and post oak underneath, unable to endure the changed 
light relations; gradually succumb. And along with the trees 
disappear also the majority of the herbaceous and shrubby plants 
of the pioneer tree stage. 

For a time the forest which thus originates may be dominated 
to so marked a degree by chestnut oak and pignut as to seem to 
warrant the recognition of a separate chestnut oak or chestnut 
oak-pignut stage in the succession.* But on the whole it 
seems simpler to regard this phase as merely a subdivision of a 
larger association which may be designated the oak-hickory 
stage. For, during the transition from the open, grove-like type 
of woodland to the closed type, other species of oak and hickory 
become increasingly abundant, so that the resultant forest 
comprises an admixture of a number of species of oak and hickory, 
together with certain other trees. The more important trees 
present in such a society are here listed. 


Acer rubrum Quercus alba 
Carya alba Quercus coccinea 
Carya glabra Quercus Prinus 
Carya ovata Quercus rubra 
Pinus Strobus Quercus velutina 


Such a forest approximates closely the type of habitat so com- 
monly referred to in the manuals as ‘“‘dry woodlands.” 
The general aspect of these oak-hickory forests at their best 


* Tt should be remarked, however, that the particular species of oak and hickory 
here mentioned by no means invariably play the important réle in the inaugura- 
tion of the oak-hickory stage that is here assigned them. Quite as often other 
species, e. g., Carya ovata, Carya alba, Quercus velutina, Quercus coccinea, are more 
prominent at the outset. 


— 
~I 
lor) 


is well brought out in fig. 3. Underneath the canopy formed by 
the larger trees there usually develop certain smallet arborescent 
species, viz., Cornus florida, Ostrya virginiana, and Sassafras 
variifolium. The rest of the undergrowth, with the exception of 
some few species like the huckleberry and the blueberries, which 


Fic. 3. An oak-hickory forest of a vezy mesophytic type; Salisbury. The 
tree in the right foreground is Quercus alba; most of the others are Quercus rubra. 
The undergrowth includes many of the shrubs listed on page 177. A majority of the 
young trees are Castanea dentaia (i. e., in center foreground) and Acer saccharum. . 


flourish equally well in the open or in diffuse light, is made up 
largely of plants which heretofore either have not been present 
at all, or else have been poorly represented in the succession. 
As representative of the shrubs may be cited: 


177 


Corylus americana Rhododendron nudifiorum 
Gaylussacia baccata Vaccinium pennsylvanicum 
Kalmia latifolia Vaccinium vacillans 


Viburnum acerifolium 


Prominent among the herbaceous plants of this stage are: 


Aspidium marginale Lysimachia quadrifolia 
Aster divaricatus Maianthemum canadense 
Carex virescens Melampyrum lineare 
Chimaphila umbellata Mitchella repens 
Cypripedium acaule Panicum dichotomum 
Desmodium sp. Pedicularis canadensis 
Epigaea repens Polystichum acrostichoides 
Gaultheria procumbens Pteris aquilina 
Geranium maculatum Pyrola americana 
Gerardia flava Pyrola elliptica 
Hepatica triloba Smilacina racemosa 
Hieracium venosum Solidago bicolor 


Solidago caesia 


Oak-hickory forests like the one here depicted constitute the 
most familiar type of woodland encountered along the trap ridges 
near New Haven, and in many sites they may represent the 
ultimate formation. But, under favorable conditions, such a 
forest is destined to give way to a still more mesophytic type. 
And here again the light requirement of the various trees involved 
seems to be an important factor in determining their behavior 
and in conditioning their presence or absence in the ultimate 
forest. For it is self evident that trees like the chestnut oak 
and pignut, whose seedlings are unable to develop in any but the 
lightest shade will tend to become less and less abundant as the 
forest floor becomes more deeply shaded by the ever denser 
foliage overhead. Conversely, it is those trees whose seedlings 
are best able to develop under these circumstances that will 
ultimately survive. Thus it comes about that the climax forest 
of any region is composed very largely of those native trees which 
are most tolerant of shade. Of course the proximate composition 
of the forest in any given locality is necessarily influenced by the 


178 


fortuitous distribution of seeds. Moreover, the advent of the 
ultimate stage may be hastened or retarded by the abundance or 
scarcity of water in the superficial layers of the soil. Thus shade 
conditions in an oak-hickory forest favor the conservation of the 
soil water, but at the same time the demands of the trees upon 
the available supply may be so great as to practically exhaust 
the water near the surface. And where, as along the summits of 
the trap ridges, water is never very abundant, it is not surprising 
to find that while the arborescent species in the forest, with their 
deeply penetrating root systems, may be relatively mesophytic, 
the shrubs and herbaceous plants, with their shallow root systems, 
are quite xerophytic. The point to be emphasized in this 
connection is that, although the mature trees of the climax forest 
may be able to utilize water at some depth below the surface, 
their seedlings are dependent on the supply near the surface; so 
that, unless there is sufficient water in these surface layers to 
enable the climax trees to tide over the critical seedling stages, 
they cannot establish themselves and the oak-hickory stage may _ 
be of indefinite duration. As will be brought out in a later 
paragraph, the accumulation of humus may have an important 
bearing on the phenomena of succession, particularly during 
these more advanced stages. 

Along the trap ridges the climax forest of this region is best 
developed on the lower slopes, where there is a relatively constant 
supply of ground water, available throughout the growing 
season.* By far the most abundant and most characteristic 
tree here is the chestnut (Castanea dentata). With it are com- 
monly associated Liriodendron Tulipifera and some of the more 
mesophytic trees of the preceding stage, e. g., Quercus rubra, 
Quercus alba, and Acer rubrum, while scattered through the forest, 
sometimes abundant locally, are other mesophytic trees, such as 
Acer saccharum, Fagus grandifolia, Fraxinus americana, Prunus 
serotina, Tilia americana, and Tsuga canadensis. As species of 
secondary importance may be mentioned Carpinus caroliniana, 

* Tt should perhaps be remarked at this point that the slopes of the trap ridges, 
especially toward the base, are usually covered to a greater or less degree with 


glacial debris. As will be brought out in a later paragraph, this fact has an im- 
portant bearing on the rapidity of the succession. 


179 


Cornus florida, Ostrya virginiana, and Sassafras varufolium. 
These are sometimes so abundant as to produce a distinct 
stratum of vegetation. Many of the shrubs and herbaceous 
plants of the oak-hickory stage are still prominent, but their 
number is augmented by numerous new arrivals, among which 
are many pronounced shade plants. Three species comprise 
the bulk of the shrubby undergrowth, viz., Kalnua latifolia, 
Hamamelis virginiana, and Viburnum acertfolium. Some of the 
characteristic herbaceous plants not heretofore noted are given 
in the subjoined list. 


Adiantum pedatum Corallorrhiza maculata 
Aspidium noveboracense Epifagus virginiana 
Aspidium spinulosum Epipactis pubescens 
Botrychium virginianum Medeola virginiana 
Lycopodium lucidulum Monotropa uniflora 
Phegopteris polypodioides Polygonatum biflorum 
Arisaema triphyllum Sanicula marilandica 
Aster dwaricatus Solidago latifolia 
Brachyelytrum erectum Trientalis americana 
Collinsonia canadensis Trillium cernuum 


Trillium erectum 


A series of changes in vegetation such as has been described in 
connection with the succession on the trap ridges is actuated 
almost entirely by biotic agencies and is therefore termed a 
biotic succession. The general manner in which biotic agencies 
institute succession has been admirably summarized by Cowles,* 
and some of his observations may be briefly stated here. All 
external factors which affect the plant reside either in the soil 
or in the air. Of the soil agencies humus is by far the most 
important in influencing succession. Due to its great capacity 
for water retention the accumulation of humus on uplands causes 
an increase in soil moisture; while in depressions, for obvious 
reasons, it has the opposite result. The change thus brought 
about in the water content of a soil is without doubt the most 
important effect of humus, and, in the opinion of Cowles, is 
perhaps the most significant of all factors influencing succession. 


* TOIT, op. cit. 


180 


Humus accumulation is associated with an increase of saprophytic 
soil organisms, a fact which may be of vital significance in con- 
ditioning the presence or absence of plants which are dependent 
on root fungi for their nitrogen supply.* The effect of humus 
on the toxicity of the soil, while as yet inadequately investigated j 
may prove to be a factor of large significance. Finally, the 
accumulation of humus modifies the soil temperature and the 
air content of the soil. 

Just as the soil factors that influence succession may be summed 
up under humus, so the air factors may largely be included under 
the head of shade. Decrease in light, as already demonstrated, is 
favorable to species tolerant of shade, but fatal to light-requiring 
species. Moreover, increased shade favors the more rapid 
accumulation of humus; it also results in increased atmospheric 
humidity, and hence in decreased evaporation. This latter 
effect is important, not only in connection with the conservation 
of soil moisture, but also as it affects the transpiration of the 
plants themselves. 

Two other biotic agencies are of greater or less importance in 
their effect on the trend of succession. The first of these is plant 
invasion. ‘‘In the long period of geologic history, plant mi- 
grations from one region to another must have played a tre- 
mendous part in the changing aspect of vegetation.”’ But, “so 
imperceptibly do these migrations take place that we know of no 
profound change that has been wrought by this means in natural 
floras within historic time.’ To this latter statement it may be 
that the chestnut blight (Endothia gyrosa var. parasitica (Murr.) 
Clint.) will furnish an interesting exception. For although much 
has been written regarding this disease from a pathological and 
an economic standpoint, it seems to the writer that its possible 
significance has been overlooked by ecologists. The chestnut 
is one of the most important trees in the climax forest, not only 
over a large part of Connecticut, but throughout much of the 


* It should be noted in this connection that recent investigations of W. B. 
McDougall (Amer. Jour. Bot. 1: 51-74. pl. 4-7 +f. I. 1914) would seem to 
indicate that the benefits accruing to many trees from their association with root 
fungi may have been greatly overestimated. 

7 Cowles, I91t. Ob. cit., p. 179. 


181 


> 


eastern United States. During the ten years that have elapsed 
since the chestnut disease was first recorded in this country— 
at New York—it has spread with amazing rapidity. At the 
present writing practically all the chestnut in southwestern 
Connecticut has been wiped out, and there is no part of the state 
which has been immune from its depredations. In the vicinity 
of New Haven much of the chestnut has already been exterminated 
and it is difficult to find a group of trees, some of which have not 
been affected by the ravages of the blight. And whether, as 
some workers think, the blight fungus is a native species, ‘‘which, 
because of peculiar conditions detrimental to the host, has 
assumed unusual virulence and widespread prominence,’’* or, 
as others maintain, is an invader from the Old World, certain it 
is that from the present outlook it is destined to have a profound 
effect on the nature of the climax forest in the eastern United 
States. 

The influence of man on succession is almost invariably retro- 


Sressive. Man destroys the more ultimate societies and causes 


them to be replaced by more primitive ones. The cutting of the 
forest, the introduction of grazing animals, and fire—all of these 
interfere with the mesotrophic trend of succession. Thus in a 
recently cleared area mesophytic herbaceous plants are largely 
superseded by the so-called “ fire-weeds’’, e. g., Epilobium angus- 
tufolium, Erechtites hieracifolia, Erigeron canadensis, Phytolacca 
decandra, and Verbascum Thapsus; while Betula populifolia, 
Myrica asplentfolia, Populus grandidentata, Populus tremuloides, 
Prunus virginiana, Rubus allegheniensis, Rubus idaeus var. acu- 
leatissimus, and other woody plants not represented in the ante- 
cedent forest may be abundant here. Fire, perhaps, should be 
considered a natural agency, but as a rule its frequency becomes 
much greater with the advent of man into a region. 

There is one other phase of succession on trap to which, as yet, 
no reference has been made, viz. succession on talus slopes. This 
is of peculiar interest because it differs in certain respects from 
the type described above. Takenasawhole the trap ranges extend 
from north to south. As a rule the hills dip gently toward the 


* Clinton, G. P. Chestnut bark disease. Report Conn. Agr. Exp. Sta. 1912: 
350-453. pl. 21-28. 1014. 


JP 


182 


east, and it is largely from a study of the vegetation on these 
slopes that the observations thus far recorded have been made. 
But toward the west the ridges terminate in perpendicular cliffs, 
at the foot of which are great masses of rocks waste (fig. 4) or 
talus, derived from the disintegration of the overhanging pre- 
cipices, and sometimes these are so extensive as to completely 
bury cliffs several hundred feet in height. The upper part of 
such a talus slope is steep, and, except at the very foot of the 
cliff, is composed of large, loose blocks of rock, with practically 


Fic. 4. Talus slope along west face of West Rock ridge, Wocdbridge. A short 
‘distance to the north of where this picture was taken the talus has become com- 
pletely covered with forest. 


no soil between them. But as the bottom is approached the 
gradiant becomes gentler, the rock fragments smaller, and a rich 
soil collects. Here conditions are favorable for plants from the 
very outset, since seepage water is abundant the year round and a 
measure of protection from wind is afforded by the neighboring 
hill. Succession proceeds with great rapidity, and the pioneer 
associations quickly give way to forest. The mesophytism of 


185 


the forests which ultimately clothe these lower slopes is attested 
by the presence of such trees as Acer saccharum, Betula lutea, Tilia 
americana, and Tsuga canadensis; also by the frequency of many 
mesophytic shrubs and herbaceous plants elsewhere uncommon 
in upland woods. Such, for example, are Actaea rubra, Asarum 
canadense, Caulophyllum thalictroides, Dicentra Cucullaria, Ge- 
vanium Robertianum, Sambucus racemosa and Staphylea trifolia. 
A further step in the reclamation of the talus by vegetation is 
seen in the appearance of a belt of trees along the upper margin 
of the slope. Here, under the very shadow of the precipice, is 
usually a narrow zone where earth and finer rock particles, dis- 
lodged from the cliff overhead, collect in sufficient quantity to 
favor rapid colonization by plants. Moisture relations, however, 
are poorer than at lower levels, so that a truly mesophytic vege- 
tation is slow to develop. The belt of forest which fringes the 
upper margin of the talus shown in fig. 4 consists largely of 
chestnut oak and black oak. But the condition shown in this 
photograph is by no means permanent. For, as the blocks of 
rock midway up the talus gradually disintegrate and soil collects, 
the two belts of forest encroach upon the barren area which 
separates them, and ultimately the entire slope becomes wooded. 
The first plants to appear in the talus succession are lichens, but 
their influence on later stages is negligible, for they are confined 
principally to the rock face while the transformations that cul- 
minate in the formation of forest are brought about almost en- 
tirely by crevice plants. Crevice mosses doubtless aid in the 
accumulation of soil and humus, and many of the crevice plants 
previously noted are also present here; but the first conspicuous 
crevice stage on talus slopes is usually dominated by vines and 
shrubs. The shade produced by trailing vines such as Celastrus 
scandens, Psedera quinquefolia, and Rhus Toxicodendron may be 
a factor of considerable significance in hastening the advent of 
mesophytic conditions. Characteristic pioneer shrubs are Cornus 
circinata, Rubus odoratus and various species of Rhus. Theshrubs 
and vines are accompanied by trees, but except toward the top 
of the slope there may never be a xerophytic pioneer tree stage, 
for among the first trees to appear may be mesophytic species 


184 


like Betula lutea, Juglans cinerea, Tilia americana, and even 
Tsuga canadensis, most of which are present in the ultimate 
forest. . 

The complexity of the surface geology of this state has been 
referred to in a previous paper.* Most of the underlying rocks 
are covered with sand, gravel, or clay; but in addition to the 
trap rocks—basalt and diabase—the surface outcrops include 
granites, gneisses, schists, quartzite, sandstone and shale, and 
limestone. To what extent, it may be asked, do the successional 
phenomena on these other types of rock correspond with, or 
disagree from, succession on trap? In other words, how is 
succession influenced by the physical or chemical nature of the 
substratum. In the opinion of Cowlest the most important 
feature of a rock, as regards its effect on succession, is its sta- 
bility, 2. e., its degree of resistance to erosion. On stable uplands, 
where erosion is slow, succession is likewise slow. On unstable 
uplands, on the other hand, succession is rapid. Thus “in a 
given region a shale area may be clothed with a mesophytic 
forest, while a dolomite outcrop is still xerophytic, or a quartzite 
is scarcely more than a naked hill.” The influence of the physio- 
graphic state of a region on the character of the vegetation is far 
more important than either the physical or chemical nature of 
the underlying rock. ‘‘The flora of a youthful topography in 
limestone more closely resembles the flora of a similar stage in 
sandstone than [that of] a young limestone topography resembles 
[that of] an old limestone topography.” In other words, ‘‘rock 
as such, or even the soil which comes from it, is of less imsportance 
in determining succession than are the aerial conditions, especially 
exposure. And it is the stage in the topography that determines 
the exposure.”’ . 

In view of Cowles’s conclusions, which are based on the study 
of succession in various parts of the eastern United States, it is 
not surprising to find that in comparing successions on different 
types of rock in this state the resemblances are much more pro- 

* Torreya 13: 109. 1913. 

7 Cowles, H. C. The influence of underlying rocks on the character of the 


vegetation. Bull..Amer. Bur. Geog. 11: 1-26. f. r-10. 1901; Bot. Gaz. 31: 890, 
90. Igor. 


185 


nounced than the differences. Thus a succession on granite, 
such as may be studied to advantage on the numerous islands 
that rise out of the salt marshes in the vicinity of New Haven, 
is strikingly similar, except in minor details, to that observed 
on trap.* 

The effect of the chemical nature of the substratum on vege- 
tation has been the occasion of much debate. A few years since, 
Fernald} made extensive investigations of arctic and alpine 
plants in the northern United States and Canada, and found that 
their distribution is controlled very largely by the preponderance 
in the soil of potassium, calcium, and magnesium. The plants 
which he studied grow mainly on the faces of cliffs, in rock 
crevices, or on talus slopes, localities where the soil is derived 
primarily from the rock in place, so that his conclusions possess 
unusual value. So far as the rate of succession is concerned, the 
chemical nature of the underlying rock would appear to be most 
important as it affects the rapidity of erosion. But it cannot be 
doubted that to a certain extent the specific composition, especi- 
ally of the earlier rock face and crevice stages, is modified directly 
by the abundance or scarcity of certain chemical elements in the 
soil. In Connecticut the problem is complicated by the fact 
that so much of the soil is of glacial or alluvial origin, and except 
in a superficial wayt this problem has not been investigated. 

In physical structure unconsolidated rocks like gravel, sand, 
and clay contrast sharply with consolidated rocks like granite 
andtrap. That this dissimilarity in the nature of the substratum 
should be reflected in the character of the vegetation is naturally 
to be expected; yet the differences are less marked than one might 
be led to anticipate. Asa concrete illustration of a succession on — 
uncompacted rock the sand plains succession has been selected. 
W.E. Britton§ has given an interesting account of the vegetation 
of the North Haven sand plains, devoting special attention to 
certain desert-like areas and the structural peculiarities of the 

* Compare Cowles, Bull. Amer. Bur. Geog. I: 14. I9QOI. 

} Fernald, M. L. The soil preferences of certain alpine and subalpine plants. 
Rhodora 9: 149-193. 1907. 


t See Torreya 13: I0Q-I1I0. I0913. 
§ Bull. Torrey Bot. Club 30: 571-620. pl. 23-28. 1903. 


186 


plants inhabiting them, but except in a general way the subject 
of plant societies was not considered. These sand plains are a 
conspicuous feature of the central lowland of Connecticut. From 


a physiographic standpoint they represent outwash plains, de- 
veloped during the final retreat of the continental glaciers, and 
now considerably dissected by stream erosion. One series of 
these plains stretches northward from New Haven, along the 


Fic. 5. Vegetation of sand plains in late summer, North Haven. The plant 
so common on the sand here’is- the annual, Trichostema dichotoma. Note the 
greater abundance of this plant in the wagon ruts—perhaps due to more favorable 
moisture relations there.. In the right foreground are Andropogon Scoparius and 
Asclepias syriaca. | 


east side of the Quinnipiac River, for about sixteen miles. The 
soil varies in texture from sand of medium fineness to coarse 
gravel. Moisture is more or less abundant throughout the year 
at a short distance below the surface, but, except in moist weather, 
the superficial soil layers are dry. This latter fact, coupled with 
wind sweep, the burning heat of the sun on the sand, and the high 
rate of evaporation, hinders the establishment of vegetation. 
The greatest divergence in plant succession on such an area 


187 


from, é. g., succession on trap is seen in the earlier, pioneer stages. 
Crustose and foliose lichens are never present—a statement which 
holds true for unconsolidated rocks in general. The first stage 
in the sand plain series may not inappropriately be termed an 
edaphic desert. The soil lacks humus and the vegetation is very 
open, the plants growing scattered about over the otherwise bare, 
sandy soil (figs. 5, 6); and since the distinctive species are either 
annuals or rhizome perennials (or biennials), there are seasons 


of the year when to all appearances these tracts are almost des- 


Fic. 6. Sand plains with scattered tufts of Andropogon scoparius; North 
Haven. Most of the trees are black oaks. Photograph after W. E. Britton. 


titute of vegetation. Here and there, however, distributed at 
irregular intervals over the surface of the plain, are trees (most 
commonly Quercus velutina) whose presence may doubtless be 
attributed to the activities of squirrels since, despite the abund- 
ance of seeds with which the ground underneath the trees is 
strewn every fall, they exhibit no tendency to spread.* 


* The acorns ‘‘fall upon the sand under the trees, probably germinate and dry 
up before the radicles can reach a sufficient depth to obtain the necessary water. 
In some unpublished investigations Prof. J. W. Toumey has found that in hard 
soil the radicle is not able to work its way into the soil, but on account of the 
lightness of the acorn it is tumbled about on the sand”’ (Britton, op. cit., pp. 
578, 579). 


188 


Two annual species are especially characteristic of such areas, 
viz. Hypericum gentianoides and Trichostema dichotomum. Asso- 
ciated with these may grow Asclepias syriaca, Baptisia tinctoria, 
Helianthemum majus, Lespedeza capitata, Oenothera biennis, Poly- 
gonella articulata, Stenophyllus capillaris and occasional repre- 
sentatives of the succeeding stage in the succession. These 
barren tracts are often quite extensive, one area near North 
Haven, according to Britton, covering from 80 to 90 acres. 

Tufts of bunch grass (Andropogon scoparius) are always more 
or less in evidence on these barrens. At first widely scattered, 


Fic. 7. Edaphic prairie; North Haven. The predominating plant is Andro- 
pogon scoparius. The dark patches near the center of the picture are shrubs— 
Myrica asplenifolia and Myrica carolinensis. All of the herbaceous species listed 
on page 189 could probably be found here. , 


they may gradually become more numerous (fig. 6) so that 
eventually, as more and more soil is preempted, a permanent 
plant cover is established. Other plants beside the bunch grass 
may fulfil an important role in the reclamation process, notably 
the moss, Polytrichum piliferum, and species of Cladonia (e. g., 
C. sylvatica, C. papillaria). These usually appear in company 
with the bunch grass, occupying the soil between the tufts; but 
sometimes mosses or lichens alone may reclaim considerable 


189 


tracts.* The second stage in the sand plains succession is 
dominated by the bunch grass, and not infrequently the areas 
controlled by this grass are so large, and the tenacity with which 
this control is retained so great, that, in the opinion of the writer, 
they should be recognized as edaphic prairies (fig. 7). Except 
for their smaller size they resemble the well known natural prairie 
of western Long Island.t 

Beside the bunch grass and some of the species already men- 
tioned the vegetation of these prairies includes many other her- 
baceous forms, nearly all of which are perennial. The following 
species are perhaps as representative as any: 


Artemisia caudata Lupinus perennis 
Asclepias verticillata Lysimachia quadrifolia 
Aster linarufolius Panicum depauperatum 
Carex Muhlenbergu Poa compressa 
Cyperus filiculmis var. Potentilla canadensis 
macilentus Pteris aquilina 

~ Desmodium canadense Rumex Acetosella 
Eragrostis pectinacea Sericocarpus asteroides 
Erigeron canadensis Solidago nemoralis 
Fragaria virginiana Viola fimbriatula 


Also two low shrubs, Myrica asplenzfolia and Rubus villosus, are 
almost invariably present and seem to form a constituent part 
of the prairie vegetation. 

Sooner or later grassland is destined to be replaced by forest. 
Sometimes a short-lived shrub stage intervenes, but quite as 
often shrubs and trees appear at about the same time. Most of 
the shrubs listed in connection with the shrub stage of the trap 
rock succession are represented in the corresponding phase of 
the sand plains succession, while several species not there men- 
tioned may also be prominent, e. g., Juniperus communis, Kalmia 
angustifolia, Myrica carolinensis, and Rhus Toxicodendron. The 
pioneer trees include Juniperus virginiana, Betula populifolia, 
Pinus rigida, and Robinia Pseud-Acacia. The last named species 

* See Britton, op. cit., p. 579. 


7 See Harper, R. M. The Hempstead Plains of Long Island. Torreya 12: 
277-286. f. I-7. 1912; also Bull. Am. Geog. Soc. 43: 351-360. f. I-5. IQII. 


190 


is native farther south, but in Connecticut has become thoroughly 
established on the sand plains and elsewhere. It is the only 
example known to the writer of a recently introduced tree which 
can be considered of ecological importance. It spreads quickly, 
largely by means of root suckers, grows rapidly, and frequently 
forms light forests over considerable areas. As a rule, however, 
the red cedar, gray birch, and pitch pine are the first arborescent 
forms to appear. These may come in together, giving rise to a 
mixed growth; or one or another, according to chance, may pre- 
dominate.* Red cedar, as along the trap ridges, usually forms 
rather open groves. Gray birch (Betula populifolia) may form 
dense stands, but the trees never attain a large size. Pitch pine 
alone, of the three, is capable of developing forests, and where this. 
species predominates, the pioneer tree stageis apt to be of much 
longer duration than otherwise. Fig. 8 shows a pitch pine stand 
near Farmington. Some of the trees here are over 18 inches in 
diameter. Theslight shade produced by the foliage overhead here 
is not sufficient to exclude from the ground underneath many of 
the herbaceous and frutescent forms characteristic of the pre- 
ceding stages, but along with these occur some species which 
attain their optimum development under more mesophytic 
conditions. The ultimate fate of a forest like this is suggested 
by the predominance on the forest floor of oak seedlings and the 
scarcity of pitch pine seedlings. As a matter of fact, owing to 
the ability of the pitch pine to endure fire, this particular forest, 
which is situated along the railroad, will probably continue 
indefinitely in its present condition. But under normal con- 
ditions oak and hickory would succeed the pitch pine, and there 
seems to be no reason to doubt that under favorable circum- 
stances the forest might at some future time become quite as. 
mesophytic as the climax type described in connection with the 
trap rock succession. 

* According to R. C. Hawley and A. F. Hawes (Forestry in New England, 
p. 352. New York. 1912), “gray birch is a species which requires a bare soil 
for a seed bed, while red cedar can start well under more adverse conditions, 
even in a thick sod. This difference in the habits of the two species explains. 


why pure stands now of one species and then of the other are met with on old 
fields.”’ 


OL 


The sand plains succession may be regarded as fairly repre- 
sentative of succession on unconsolidated rocks. It differs in 
some respects from succession on gravel and clay, but so far as 


the sequence and composition of stages is concerned the resem- 


blances are greater than the differences. Just as was found in the 


ad Swe 


2 
ie 
5 
5 
ee 


Hie. 8: 


Pitch pine forest; Farmington. 
phytic, 


The undergrowth is largely xero- 
common shrubs being Ceanothus americana, Corylus americana, Myrica 
asplenifolia, Quercus tlicifolia and Rhus glabra. 

case of consolidated rocks, the chief difference between various 
uncompacted rocks in their effect on succession concerns the 
quickness or slowness with which mesophytic conditions are 
attained. The presence of clay in a soil increases its ability to 
retain water and thereby favors the more rapid advent of meso- 
phytism. The most favorable of all soils in Connecticut, from a 


192 


standpoint of natural vegetation, are the heterogeneous deposits 
of gravel, sand, and clay known as till. On such soils succession 
progresses so rapidly that, except where conditions have been 
modified by human interference, pioneer associations are seldom 
encountered. It should also be mentioned at this point that 
frequently, due to the influence of soil structure or ground water ~ 
relations, swamps may be developed on uplands. But from an 
ecological standpoint these are better considered in connection 
with lowlands. 

Several allusions have been made to the effect on vegetation 
of human interference. Unfortunately for the ecologist this is a 
factor which too often must be reckoned with. There is one type 
of succession resulting from man’s activities which is deserving 
of special mention because of its widespread occurrence, viz., 
ruderal succession.* Whenever a plowed field is allowed to lie 
fallow for a year, a ruderal association arises. At first the plant 
population of such an area is composed largely of weeds, many 
of which are annuals. Of these, Ambrosia artemisifolia is almost 
omnipresent, but it is hardly worth while to attempt a represen- 
tative list of the others. It may be noted in passing, however, 
that among the mosses some forms like Funaria hygrometrica and 
Physcomitrium turbinatum should be classed as weeds. If a 
field is permanently abandoned perennial herbaceous plants 
soon form a sod, so that annual species are largely excluded, and 
woody plants begin to assert themselves. In this way there may 
originate the type of vegetation known to the forester as the 
“‘old field type.”’ This type is a common one in abandoned 
pastures, constituting one of the most familiar features of a 
Connecticut landscape. The characteristic trees are usually gray 
birch and red cedar, with which are associated low juniper and 
many other pioneer shrubs (fig. 9). If left to themselves such 
areas, in the course of time, may become clothed with meso- 
phytic forests. 

Taken as a whole, the observations recorded in the preceding 
paragraphs are applicable to upland vegetation in any part of 
Connecticut, but there are a few noteworthy discrepancies. The 
earlier stages in the succession are essentially alike everywhere, 


* See Clements, F. E. Research methods in ecology, p. 253. Lincoln. 1905. 


193 


although there may be some divergence in the shrub stage, due 
to the local abundance or scarcity of particular species. But the 
tree stages in different sections exhibit some appreciable dis- 
similarities. Reference has been made in previous papers* to 
variations in the composition of the climax forest. The earlier 
tree stages as well manifest certain differences. Gray birch is a 
common pioneer tree in all sections, but post oak is confined to 


Fic. 9. A typical ‘“‘old field’’ society in an abandoned pasture; New Haven. 


Juniperus virginiana and Juniperus communis var. depressa. 


the proximity of the coast, and even here it is quite re- 
stricted in its distribution. Red cedar and pitch pine are rel- 
atively rare in northwestern Connecticut, but they are common 
elsewhere. Of the two, red cedar is the more usual pioneer in 
the southwestern part of the state; in the central lowland and 
jn eastern Connecticut both are locally important. The aspens 
(Populus tremuloides, P. grandidentata) are of sporadic occurrence 
throughout, especially in areas recently burned over, but they 


* Torreya 13: 99, IOI; 199-215. 1913; Bot. Gaz. 56: 143,144. I913. 


194 


are perhaps more conspicuous as pioneers in northwestern 
Connecticut than elsewhere. The paper birch (Betula alba 
papyrifera), also, is not an infrequent pioneer in Litchfield 
County and along the trap ridges toward the north, but is rare 
near the coast. The most striking departure, however, from 
any type of succession heretofore described is seen where the 
pioneer tree is the white pine (Pinus Strobus). The white pine 
is widely distributed throughout the state, but its ecological 
importance varies. Over much of southwestern Connecticut it 
is so uncommon as to be a negligible factor as regards its influence 
on succession; and while frequent enough in the southern part of 
the central lowland it usually grows scattered and intermixed 
with other trees. But in parts of northern and eastern Con- 
necticut the white pine predominates over considerable areas and 
is a common pioneer in abandoned fields and cut-over tracts. 
Where white pine comes in strongly—frequently forming, as it 
does, nearly pure stands—the oak-hickory stage in the succession 
is often completely eliminated. There may thus be only two 
tree stages, pine remaining dominant until largely superseded 
by the more tolerant species of the climax forest. The white 
pine may even be represented in this ultimate forest, in this 
respect differing from any other pioneer tree. The undergrowth 
in evergreen, coniferous forests is much sparser than that of 
deciduous forests, owing to the dry carpet of needles with which 
the ground is littered. But practically all the shrubs and herbs 
characteristic of oak-hickory forests are to be found in many 
white pine forests. On the whole, therefore, it seems appropriate 
to regard such forests as ecologically equivalent to the oak- 
hickory forests developed elsewhere. 


SHEFFIELD SCIENTIFIC SCHOOL OF YALE UNIVERSITY 


195 


ALGAL STALACTITES IN BERMUDA 


By JoHN W. HARSHBERGER 


The hills of Bermuda are formed of a friable limestone, which 
represents particles of calcareous sand, which in the early geologic 
history of this group of islands was drifted by the wind into 
elevated dunes and afterwards by water action was compacted 
into a harder, or a softer, lime rock. This native rock is sawed 
out of the hillsides and is used in the construction of house. 
walls (large, thick blocks), or house roofs (large, thin slabs). 
When exposed to the air, this soft quarried rock hardens into a 
form of limestone, much like concrete in appearance. As in all 
limestone formations of any considerable thickness, caverns and 
underground tunnels are worn into the softer strata by the action 
of rain, and underground water. Several caverns of this char- 
acter are visited by tourists in Bermuda and some of them have 
pools of salt-water replenished by underground supplies from the 
ocean. There are limestone sinks, which represent caves, the 
toofs of which have fallen in. A number of these sinks are dry, 
others are filled with water. One of the most frequently visited 
of these depressions, filled with saltwater, which comes under- 
ground from the ocean, is Devil’s Hole in which are kept a 
number of the characteristic fishes of the Bermuda archipelago, 
such as, the grouper, the angel-fish, the red-snapper and others 
equally celebrated. The walls of the Devil’s Hole are rather 
steep, and in places overhanging, so that the fresh water from the 
rocks above drips into the pool beneath. Here were found 
stalactites from an inch to two inches in length and coated with a 
covering of blue-green algae. 

Several of these stalactites were broken off from the overhanging 
wall in Devil’s Hole, June, 1905, and kept dry for subsequent 
study, but the material was overlooked until the present summer 
(1914), when a study was made of it. Small pieces of stalactite 
were crushed in water and examined under the microscope. The 
blue-green algae, which alone were present, were identified with 
Josephine Tilden’s* first volume of Minnesota Algae. The algae 


* Tilden, Josephine. Minnesota Algae. Volume I. The Myxophyceae of 
North America and Adjacent Regions, including Central America, Greenland, 
Bermuda, the West Indies and Hawaii. Bot. Ser. VIII, Igto. 


196 


found on this examination consisted of Chrootheca Richteriana 
Hansg., Gleocapsa aeruginosa (Carmichael) Kuetzing, G. gelatinosa 
Kuetzing, G. quarternata (Brébisson) Kuetzing and Gleotheca 
linearis Naegeli. Attached to a small red alga (not identifiable) 
which was fastened to a piece of stalactite was found Microcystis 
flos-aqua (Wittrock) Kirchner. The most abundant blue-green 
alga was Chrootheca Richteriana Hansg., which, according to 
Josephine Tilden, consists of a somewhat gelatinous plant mass, 
thick, or more or less expanded of a blue-green, or yellowish color. 
The cells found in these masses are 18-24 microns in diameter, 
once to twice as long as wide, single, or in pairs, with thick sheaths 
up to 6 microns in diameter. This species, figured by Miss 
Tilden, has been reported from Bermuda by Farlow and from 
Montego Bay, Jamaica, by Pease and Butler. Of the three 
species of Gleocapsa enumerated above, the following is the 
distribution recorded in the Minnesota Alge: 

G. aeruginosa Greenland, New York, West Indies (Porto Rico). 

G. gelatinosa United States, West Indies. 

G. quarternata West Indies, Hawaii. 
The note with reference to G. aeraginosa in Minnesota Algae is 
apropos: ‘West Indies. Forming a dark green layer on stone 
incave. ‘El Convento,’ near Penuelas, Porto Rico (Sintenis) ’”” 
Gleocapsa quarternata is described as forming a gray-green, muci- 
laginous coating on wet cliffs in Hawaii. The distribution of 
Gleotheca linearis is given in Minnesota Algae, as: ‘‘West Indies. 
On damp walls of dam, Sharp’s River, St. Vincent (Elliott).” 

That these algae are active in the formation of the stalactites 
is indicated by their close attachment to the surface of the sta- 
lactites in the Devil’s Hole, Bermuda. They remove in the 
case of the carbonated waters, containing calcium bicarbonate 
(CaHCOs). in solution, the gaseous carbon dioxide, which is. 
used by the blue-green algae in photosynthesis of organic com- 
pounds, so that the stalactites are formed by the continual 
deposit of calcium carbonate (CaCQO3). Josephine Tilden has. 
studied the formation of algal stalactites in the Yellowstone 
National Park, where such algae as Gleocapsa violacea, Phormidium 
(Leptothrix) laminosum, Schizothrix calcicola and Synecococcus 


19 


aeruginosus are active. Associated with the older part of the 
Bermuda stalactites, I found a small gasteropod mollusc, (Kaliella 
turbinata Gulick), hid away in small holes, or irregularities of their 
surface. In conclusion, we find by the study of the material 
from Bermuda, that other algae are concerned in the formation of 
stalactites besides those described from Yellowstone Park, and 
if a comparative study were made of stalactitic material from all 
parts of the world, the writer has no doubt that the list of algae 
concerned would be a respectable one. 


ON ERIGERON PUSILLUS NUTT. 


By N. L. BRITTON 


I was much interested in reading Dr. B. L. Robinson’s remarks 
on this species published in Rhodora for December, 1913, and, 
especially, because it was the study of specimens from Bermuda 
which enabled him to recognize the difference between this 
species and FE. canadensis L. During a visit to Bermuda in late 
May and early June of this year, in company with Mr. Stewardson 
Brown, we studied these plants in the field, and our observations 
led us to agree with Dr. Robinson in ability to recognize the 
two species without any difficulty whatever, Mr. Brown having 
previously had similar experience in southern New Jersey. From 
the standpoint of the Bermuda flora, my interest in this plant 
was again increased because Mr. Oswald A. Reade, in his ‘‘ Plants 
of Bermuda,” published in 1883, had recorded both canadensis 
and pusillus from these islands, although not very well expressing ~ 
the characters of pusillus, which he regarded as a dwarf state of 
canadensis; the purple-tipped involucral bracts, first observed 
by Dr. Robinson and cited by him as the salient character, are 
constant in Bermuda and, apparently, throughout the range of 
the plant in the eastern United States, as also the glabrate 
feature, entire leaves and smaller size of E. pusillus. In Bermuda, 
the two plants grow side by side in fields and along roadsides, and 
in some localities, at least, are equally abundant. Intermediate 
stations between Rhode Island and South Carolina are Bayshore, 
Long Island (John McCallum), Belmar, Monmouth County, 


198 


New Jersey (Taylor 1450) and New Egypt, Ocean County, New 
Jersey (Taylor 2650), several localities in Cape May County, 
New Jersey, and Milton, Delaware, reported by Mr. Brown. 
Additional West Indian stations are Great Bahama (Brace 3685, 
Britton & Millspaugh 2703 and 2445); Abaco (Brace 1827 and 
1864); Andros (Brace 6996 and 7127); North Caicos (Millspaugh 
9179); St. Thomas (Eggers); Santo Domingo (Fuertes go); 
Porto Rico (Heller 1350); Vieques (Shafer 2619A); Montserrat 
(Shafer 14); St. Kitts (Britton & Cowell 428). All the above cited 
specimens are glabrate, with purple-tipped bracts, and essentially 
entire leaves (the lower leaves of the North Caicos plant have a 
few sharp teeth). 

In studying West Indian collections, I had long ago noticed 
the glabrate feature as compared with the hirsute EL. canadensis 
of the eastern United States, and had sorted the specimens of 
our collections in accordance with this feature, but I had not 
noticed the purple-tipped involucral bracts. We have a large 
number of specimens from the West Indies which are quite as 
glabrous as those cited by Dr. Robinson as belonging to pusillus, 
and agreeing with them, apparently, in every other character 
except that of these purple tips; I cite the following as illustrating 
this series: Inagua (Nash & Taylor 1408); Hog Island, New 
Providence (Wilson 8253); Andros (Brace 4587); Great Ragged 
Island (Wilson 7877); Eleuthera (Coker 381); Grand Turk (Nash 
& Taylor 3865); Cuba (Wright 1313, Wilson 195 and 243, Britton 
& Shafer 726, O'Donovan 5251, Leon 1325, Shafer 2442, Van 
Hermann 789); Porto Rico (Britton & Cowell 1547); Mona 
(Stevens 6391); Martinique (Duss 1442); Guadeloupe (Duss 2505); 
Barbados (Botanic Station 521); Jamaica (Fredholm 3317); 
Columbia (H. H. Smith 527). It is possible that some of these 
may have shown purple-tipped involucral bracts in life, but I 
have not been able to see them in the dried specimens. 

It would seem to me probable, therefore, that the characters 
of purple-tipped involucral scales may not be constant, but 
that the species must rest on its glabrate feature, usually smaller 
size, and entire leaves. Inasmuch as I regard these plants as 
generically distinct from Erigeron, I here propose the binomial 
Leptilon pusillum. 


199 


My study of the specimens, in so far as the collections of the 
New York Botanical Garden illustrate the two species and Mr. 
Brown’s examination of the Philadelphia collections, exclude 
Leptilon canadense from the West Indies, except Bermuda, and 
also from the southeastern continental United States, south of 
North Carolina. 

The figure accompanying the description of L. canadensis in 
“‘Tilustrated Flora’’ was drawn from a specimen of L. pusillum. 


NEWS ITEMS. 


We learn from the Evening Post that Miss Flora Anderson and 
Miss Margaret DeMerritt have been appointed as instructors 
in botany at Wellesley, and that Miss Grace L. Clapp has been 
appointed to a similar position at Smith. 


Doctorates in botany were conferred at the close of the summer 
quarter of the University of Chicago upon Miss Hannah Aase of 
Washington State College, Professor J. S. Caldwell of Alabama 
Polytechnic Institute, Professor G. B. Rigg of University of 
Washington, Professor J. B. Stober, and Miss Eva Schley. 


Mr. Adolph Rolloff, director of the State Botanical Garden in 
Tiflis, Russia, is visiting the botanical gardens of the United 
States. - 


We learn from Science that Dr. J. J. Tauberhaus has been 
promoted from assistant to associate research plant pathologist 
at the Delaware College Agricultural Experiment Station. 


From the same source we learn of the death at the age of 
thirty-seven of Dr. J. E. Gow, who was professor of botany at 
Coe College. 


Mr. Guy R. Bisby who has been conducting investigations on 
the potato diseases in Maine during the past summer, has returned 
to the Brooklyn Botanic Garden. 


At the same institution Dr. R. R. Gates has registered for a 
time as an investigator and Mr. Alfred L. Gundersen has been 
appointed as assistant in the herbarium. 


200 


A new edition of the Naturalists’ Directory has just been 
published by S. E. Cassino, Salem, Mass. This directory is 
useful to naturalists since it is the means of bringing together 
students and collectors in all parts of the world through cor- 
respondence. The directory contains an alphabetical list of 
English speaking professional and amateur naturalists in all 
parts of the world, also a list of scientific societies and periodicals. 
Further information may be had from the publisher. 


An announcement has just been issued of a new paleobotanical 
bimonthly, Paleobotanischen Zentralblatt, which is to be published 
under the auspices of the Internationalen Palcobotanischen 
Gesellschaft. It is under the management of a committee, 
which in America is represented by Dr. E. W. Berry, Johns 
Hopkins University, where additional information may be 
obtained. 


The Torrey Botanical Club 


Contributors of accepted articles and reviews who wish six 
gratuitous copies of thenumber of Torreya in which their papers 
appear, will kindly notify the editor when returning proof. 

Reprints should be ordered, when galley proof is returned 

to the editor. The New Era Printing Co., 41.North Queen 
| Street, Lancaster, Pa., have furnished the following rates : 


2pp 4pp — 8pp 12pp 16pp 20pp 
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200 copies 1.70 2.35 2.90 3.75 4.35 4.70 
“Covers: 25 for 75 cents, additional covers 1 cent each. 
Plates for reprints, 40 cents each per 100. 


The following Committees have been appointed for 1914 


Finance Committee Field Committee 
J: H. Barnuart, Chairman SERENO STETSON, Chairman 
Miss C.-C. HAYNES 

Budget Committee Program Committee 4 
J. H. Barnuart,. Chairman Mrs. E. G. Brirron, Chairman 
N. L. BritTon Miss JEAN BROADHURST 
B. O. DopcGE C. STUART GAGER 
M. A. Hower F.. J. SEAVER 
A. W. Evans 
H. H. Ruspy 


Local Flora Committee 
N. L. Britton, Chairman 


Phanerogams: Cryptogams: 

E.. P. BICKNELL Mrs. E. G. BRITTON 
~N. L. Brirron Puitie DowELL 

C. €. Curtis Tracy E. Hazen 

K..K. MAcKENZIE M. A. Howe 

NoRMAN TAyYLor W. A. MurRILe 


Delegate to the Council of the New York Academy of Sciences 
WILLIAM MANSFIELD 


OTHER PUBLICATIONS — 


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3 Vol. ‘14 Ges November, Igi4 No. I1 


RREYA 


~ A Monruty Journar or Boranicat Notes anp News 


EDITED FOR 


THE ‘TORREY BOTANICAL CLUB 
BY 
NORMAN TAYLOR 
joHN TORREY, 1796-1873 
ee he ee RONTENTS 


Flora of. Southold and Gardiner’s Island: S. H. BuRNHAM AND’R. A. LATHAM...... 201 

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TORREYA 


November, Ig14. 
Vol. 14 No. 11 


THE FLORA OF THE TOWN OF SOUTHOLD, LONG 
ISLAND AND GARDINER’S ISLAND 


By STEWART H. BURNHAM AND Roy A. LATHAM 


The town of Southold is at the eastern end of the north shore 
of Long Island, extending westward for twenty miles through 
the villages of Orient, East Marion, Greenport, Southold, 
Peconic, Cutchogue to Mattituck and Laurel. The topography 
of the town affords a pleasing variation. On the north, paralleled 
with the coast of Long Island Sound, are rolling plains and 
hillocks; now forested, now barren, or broken by low-lying necks 
of sandy beaches and inlets. On the south, facing the bays and 
harbors, are extensive salt meadows drained by numerous tidal 
creeks: the marshes bordered, here and there, by.a growth of 
cedar and hardwood. Between the waterways and tidal creeks 
sandy beaches extend far out: such areas often being covered 
with sprawling red cedars, pitch pine and beach plum shrubs. 
On one of these peninsulas at Orient over seventy-five species 
of lichens have been found, growing either on the low trees or 
on the ground: and on a single prostrate cedar fourteen species 
were found. Fertile, low, level farms lie principally through the 
center of the town of Southold. Among the more common 
plants found throughout the town but not known to occur at 
Orient, are: Skunk-cabbage, beech, witch-hazel, trailing arbutus 
and mountain laurel. These plants are found at Greenport, six 
miles west of Orient: and the local flora of these two places 
seem strangely different. 

Gardiner’s Island is situated ten miles southeast of Orient and 
three miles north of the Hampton shore. The flora is quite 
similar to that found about Orient; excepting the abundance of 


No. 10, Vol. 14, of TORREYA comprising pp. 167-200 was issued 27 October 1914] 


201 


Lis 
NEW 
B0TA 
@Ak 


202 


seaside knotweed, sea purslane, sea poppy, New England aster 
and Scotch thistle. The island is still wooded with the magnifi- 
cent first-growth oak and beech forests: interposed with high 
rolling plains and rich luxuriant lowlands, side by side. 

Roy A. Latham of Orient, from May 25, 1909, until the present 
time, collected the following plants: and many of the specimens 
passed through my hands while in the State Botanist’s office at 
Albany, New York. The major part of the species here listed 
were collected between Orient and Greenport; where much of 
the region remains in its original state. A few of the best of the 
specimens are preserved in the New York State Herbarium; 
some of the poorer ones were saved; “‘scrappy’’ ones were con- 
signed to the waste basket; and several fungi were left unnamed 
or in doubt. 

The arrangement of the list accords with Dr. Smith Ely 
Jelliffe’s, The Flora of Long Island, 1899. The nomenclature 
of the Myxomycetes follows Dr. Thomas H. Macbride’s, North 
American Slime-Moulds; and that of the Algae, Dr. Bradley 
M. Davis’s, A Catalogue of the Marine Flora of Woods Hole 
and Vicinity. The nomenclature of the Fungi in most instances 
follows P. A. Saccardo’s, Sylloge Fungorum: and the authors 
are under great obligation to Dr. Charles H. Peck, State Botanist 
of New York, for helping solve many difficult problems among 
the Higher Basidiomycetes. The nomenclature of the Lichens 
conforms with a modification of the Nylander system; that of 
the Hepaticae, follows Dr. A. W. Evans: and that of the Musci, 
Dr. A. J. Grout’s, Mosses with Hand-lens and Microscope. 
The nomenclature of the ferns and flowering plants follows the 
last edition of Dr. N. L. Britton and A. Brown’s, An Illustrated 
Flora of the Northern States and Canada. 

It has seemed best not to arrange the long list of cryptogams 
according to families and increase the length of this article: 
but to list the species under botanical orders alphabetically. 
The ferns and phanerogams are arranged according to families: 
but the species are listed in alphabetical order. 


203 


INSECT GALLS* 


Acarus Serotinae Beutm.—Wild Cherry Pouch Gall. 

Acraspis erinacet Walsh—Oak Hedgehog Gall. 

Amphibolips confluentus Harr.—Oak Apple. 

Andricus futilis O. S—Oak Wart Gall on leaves of Quercus alba. 

A. palustris O. S—Succulent Oak Gall on leaves of Quercus palustris. 
A. petiolicola Bass.—Oak Petiole Gall on leaves of Quercus alba and Q. velutina. 
A. punctatus Bass.—Oak Knot Gall. 

A. seminator Harr.—Oak Seed Gall. 

Asteromyia rubra Felt—On leaves of Solidago bicolor. 

Aulax tumidus Bass.—Lettuce Tumor Gall. 

Biorhiza forticornis Walsh—Oak Fig Gall on twigs of Quercus alba. 
Cecidomyia Caryaecola O. S.—Hickory Seed Gall. 

C. holotricha O. S.—Hickory Onion Gall. 

C. niveipila O. S.—Oak Fold Gall. 

C. Nyssaecola Beutm.—On leaves of Nyssa sylvatica. 

C. (2) ocellaris Comstock—Maple Spot Gall on leaves of Acer rubrum. 
C. sanguinolenta O. S.—Hickory Cone Gall. 

C. Serotinae O. S.—Wild Cherry Bud Gall. 

Cincticornia pilulae Walsh—Oak Pill Gall on leaves of Quercus velutina. 
Cynips Pisum Fitch—Oak Pea Gall. 

Cystiphora canadensis Felt—On leaves of Nabalus. 

C. viburnifolia Felt—On leaves of Viburnum acerifolium and V. dentatum. 
Dasyneura Galii Felt—On flower buds of Galium. 

D. Salicifolia Felt—On young willow leaves. 

Diastrophus Cuscutaeformis O. S.—Blackberry Seed Gall. 

D. nebulosus O. S.—Blackberry Knot Gall. 

D. niger Bass.—On leaves of Potentilla canadensis. 

Dryophanta polita Bass.—Polished Oak Gall. 

Erineum fagineum Pers.—Beechleaf Mite Gall. 

Eriophyes abnormis Garman—A mite gall on leaves of Tilia americana. 
E. Nyssae Trotter—On leaves of Nyssa sylvatica. 

E. Querci Garman—On leaves of Quercus velutina. 

Gnorimoschema gallaesolidaginis Riley—On stems of Solidago serotina. 
Holcaspis globulus Fitch—Oak Bullet Gall. 

Hormaphis Hamamelidis Fitch—Witch Hazel Cone Gall. 

H. spinosus Shiner—Spiny Witch Hazel Gall. 

Hormomyia Crataegifolia Felt—On leaves of Crataegus. 

TItonida foliora Russ. & Hook.—On margin of leaves of Quercus velutina. 
Lasioptera farinosa Beutm.—On leaf veins of Rubus. 

L. Lycopi Felt—On stems of Lycopus. 

L. virginica Felt—On stems of Triadenum virginicum. 

L. Vitis O. S—Grape-vine Tomato Gall. 

Nemaius pomum Walsh—Willow Apple Gall. 

Neolasioptera Erigerontis Felt—On stems of Leptilon canadense. 


* The majority of these galls were named by Dr. E. P. Felt, state entomologist 
of the state of New York. 


204 


NV. vitinea Felt—On petioles of grape leaves. 

Neuroterus batatus Fitch—Oak Potato Gall on twigs of Quercus alba. 
N. majalis Bass.—On leaves of Quercus alba. 

Obolodiplosis Robiniae Hald.—On leaves of Robinia Pseudo-A cacia. 
Oligotrophus salicifolius Felt—On leaves of Salix discolor. 
Pachypsylla Celtidis-gemma Riley—Hackberry Nodule Gall. 

P. Celtidis-mamma Riley—Hackberry Nipple Gall. 

Pemphigus Populicaulis Fitch—Poplar Stem Gall. 

P. Rhois Fitch—Sumac Tomato Gall on leaves of Rhus glabra. 
Phylloxera Caryaecaulis Fitch—Hickory Louse Gall. 

P. Caryae-globuli Walsh 

P. vastatrix Planch.—Grape Phylloxera. 

P. vitifoliae Fitch 

Rhabdophaga Salicifolia Felt—On leaves of Spirea latifolia. 
Rhodites bicolor Harr.—Spiny Rose Gall. 

R. dichlocerus Harr.—Long Rose Gall. 

R. globosus Beutm.—Globular Rose Gall. 

R. ignota O. Si—Mealy Rose Gall. 

R. verna O. S.—Knotty Rose Gall. 

Rhopalomyia anthophila O. S.—On leaves of Solidago. 

R. capitata Felt—On stems of Solidago. 

R. lateriflora Felt—On stems of Aster ericoides. 

R. racemicola O. S.—On flowers of Solidago rugosa. 

Sackenomyia viburnifolia Felt—On leaves of Viburnum dentatum. 
Solenozopheria Vaccinii Ashm.—Huckleberry Gall on stems of Gaylussacia baccata. 
Trypeta polita Lw.—Goldenrod Gall. 


THALLOPHYTA 
MYXOTHALLOPHYTA 


MyYxXOMYCETES 


Arcyria cinerea (Bull.) Pers.—On rotten wood of oak. 

A. denudata (L.) Sheldon—On hickory and cherry. 

Ceratiomyxa fruticulosa (Muell.) Macbr.—On rotten wood. 

Fuligo ovata (Schaeff.) Macbr.—On old oak trunks. 

Hemitrichia serpula (Scop.) Rost.—On old hickory wood. 

H. vesparium (Batsch) Macbr.—On old hickory wood. 

Lycogala epidendrum (Buxb.) Fr.—On pine stumps, hickory and oak. 

Plasmodiophora Brassicae Woron.—On roots of Brassica oleracea; determined at 
Bureau of Plant Industry, Washington. 

Reticularia Lycoperdon Bull.—On Sassafras Sassafras: 

Stemonites Smithit Macbr.—On old logs. 

Trichia favoginea (Batsch) Pers.—On old wood of Robinia Pseudo-Acacia. 


EUTHALLOPHYTA 


- EUPHYCEAE* 
A gardhiella tenera (Ag.) J. Ag. 


Ahnfeltia plicata (Huds.) Fr. 


* The marine algae were mostly determined by Dr. M. A. Howe and are pre- 
served in the Herbarium of the New York Botanical Garden. 


205 


Anabena torulosa (Carm.) Lag. 

Antithamnion Pylaisaei (Mont.) Kjellm. 

Ascophyllum nodosum (L.) LeJolis 

Callithamnion Baileyi Harv. 

C. byssoideum Arn. 

Ceramium fastigiatum Harv. 

C. rubrum (Huds.) Ag. 

C. tenuissimum (Lyngyb.) J. Ag.—Greenport. 

Chaetomorpha Linum (Miill.) Kiitz. 

Champia parvula (Ag.) Harv. 

Chlorococcum humicola (Naeg.) Rabenh.—A fresh-water alga on a piece of wood. 

Chondria tenuissima (Good. & Woodw.) Ag. 

Chondrus crispus (L.) Stackh. 

Chorda filum (L.) Stackh. 

Chordaria flagelliformis (Miill.) Ag. 

Cladophora arcta (Dillw.) Kiitz. 

C. expansa (Mert.) Kiitz. 

C. flexuosa (Griff.) Harv. 

C. gracilis (Griff.) Kiitz. 

Corallina officinalis L. 

Cystoclonium purpurascens (Huds.) Kiitz. 

Dasya pedicellata Ag. 

Delesseria sinuosa (Good. & Woodw.) Lamour. 

Dermatolithon pustulatum (Lamour.) Fosl.—On leaves of Zostera. 

Desmarestia aculeata (L.) Lamour. 

D. viridis (Miill.) Lamour. 

Dictyosiphon foeniculaceus (Huds.) Grev. 

Ectocarpus confervoides (Roth) LeJolis 

E. fasciculatus Harv. 

FE. siliculosus (Dillw.) Ag. 

Enteromorpha compressa (L.) Grev. 

E. intestinalis (L.) Grev. 

EF. linza (L.) J. Ag. 

E. percursa (Ag.) J. Ag. 

E. plumosa Kiitz. 

Epilithon membranaceum (Esp.) Heyd. 

Fucus evanescens Ag. 

F. spiralis L. 

F. vesiculosus L. 

Gractlaria confervoides (L.) Grev. 

Gymnogongrus Torreyi (Ag.) J. Ag —Dr. Howe says: “probably only a flattened 
variety of Ahnfeltia plicata (Huds.) Fr.” 

Halothrix lumbricalis (Kiitz.) Reinke—On leaves of Zostera. 

Hildebrandia prototypus Nardo 

Hypnea musciformis (Wulf.) Lamour. 

Isactis glauca Thuret 

Laminaria A gardhii Kjellm. 

L. digitata (L.) Lamour. 


206 


Leathesia difformis (L.) Aresch.—Probably the young thalli on Zostera. 

Lithophyllum pustulatum (Lamoutr.) Fosl. 

Lomentaria uncinata Menegh. 

Melobesia Lejolisii Rosan.—On leaves of Zostera. 

Mesogloia divaricata (Ag.) Kiitz. 

Monostroma leptoderma Kjellm. 

M. undulatum Farlowii Fos!. 

Petalonia fascia (Miill.) Kiitz. 

Phyllophora membranifolia (Good. & Woodw.) J. Ag. 

Polyides rotundus (Gmel.) Grev. 

Polysiphonia elongata (Huds.) Harv. 

P. Harveyi Bailey 

P. nigrescens (Dillw.) Grev. 

P. Olneyi Harv. 

P. urceolata (Lightf.) Grev. 

P. urceolata formosa (Suhr) J. Ag. 

P. variegata (Ag.) Zanard. 

Punctaria latifolia Grev. 

Pylaiella littoralis (L.) Kjellm. 

Rhodermis Georgii (Batt.) Collins—On leaves of Zostera. 

Rhodomela subfusca (Woodw.) Ag.—Also the red form, approaching Rhodomela 
Rochei Harv. 

Rhodymenia palmata (L.) Grev. 

Sargassum Filipendula (Ag.) J. Ag. 

Scytosiphon lomentarius (Lygyb.) J. Ag. 

S. lomentarius complanatus Rosev. 

Spermothamnium Turneri (Mert.) Aresch.—Attached to the base of Polysiphonia 
elongata. 

Sphacelaria cirrhosa (Roth) Ag. 

Spyridia filamentosa (Wulf.) Harv. 

Sterrocolax decipiens Schmitz.—‘‘ Abundant on Gymnogongrus Torreyi, which fact 
may be interpreted as strengthening the idea that G. Torreyi is only a form of 
Ahnfeltia plicata.””* 

Stilophora rhizodes (Ehrh.) J. Ag. 

Ulothrix flaccida (Dillw.) Thuret 

Ulva Lactuca L. 

U. Lactuca latissima (L.) DC. 

FUNGI 
SCHIZOMYCETES 


Bacillus amylovorus (Burr.) DeToni—On leaves of Pyrus communis. 


EUMYCETES 
PHYCOMYCETES 
Bremia Lactucae Regel—On Lactuca leaves. 
Cystopus candidus (Pers.) Lev.—On Bursa Bursa-pastovis and other mustards. 


* Some Midwinter Algae of Long Island Sound, by M. A. Howe in Torreya 14: 
97-101. June, 1914 (Contr. N. Y. Botanical Garden No. 169). 


207 


Mucor Mucedo 1..—On beet stored in a cellar; determined at Cornell by Prof. 
Fitzpatrick. 
Rhizopus nigricans Ehrenb.—On stale bread. 


ASCOMYCETES (EXCLUDING PYRENOMYCETES) 


Belonidium aurelia (Pers.) DeNot.—On old wood of Robinia Pseudo-Acacia; 
specimens in N. Y. State Herbarium. 

Bulgaria inquinans (Pers.) Fr. 

Chlorosplenium aeruginosum (Oeder) DeNot.—On old wood of Acer rubrum. 

C. Schweintizi Fr. 

Coccomyces Junipert Karst.—On bark of Juniperus virginiana; specimens in N. Y. 
State Herbarium. (Colopoma Juniperinum C. & P.) 

Dasyscypha calcycina (Schum.) Fckl.—On bark of Pinus rigida. 

D. virginea (Batsch) Fckl.—On oak. 

Discina orbicularis Pk.—On old wood of hickory and cherry. 

Durella corrugata (C. & P.) Sace.—On oak twigs; specimens in N. Y. State Her- 
barium. 

Exoascus deformans (Berk.) Fckl.—On leaves of Amygdalus persica. 

F. varius Atk.—On leaves of Padus virginiana. 

Geoglossum velutipes Pk.—On ground in woods. 

Geopyxis hesperidea Cke. & Pk.—On logs; specimens in N. Y. State Herbarium. 

Gyromitra esculenta (Pers.) Fr.—Rare in cedar woods at Orient. 

Helotium citrinum (Hedw.) Fr.—On old oak and hickory wood. 

Helvella macropus (Pers.) Karst. 

Humaria granulata (Bull.) Sacc.—On cow dung and old potato stems; specimens 
in N. Y. State Herbarium. 

Lachnea scutellata (L.) Gill-—On old oak wood. 

L. setosa (Nees) Gill—East Marion on rotten stumps. 

Lecanidion indigoticum (C. & P.) Sacc.—Specimens in N. Y. State Herbarium. 

Leotia lubrica (Scop.) Pers. 

Mollisia melaleuca (Fr.) Sacc.—On old wood of Robinia Pseudo-Acacia. 

Morchella conica Pers. 

M. deliciosa Fr. 

M. esculenta (L.) Pers.—The morels all grow in sandy soil, at Orient. 

Phaeangella deformata (Pk.) Sacc. & D. Sacc.—Growing in lines on bark of Juniperus 
virginiana; specimens in N. Y. State Herbarium. 

Propolis faginea (Schrad.) Karst.—On old wood of willow and hickory; specimens 
in N. Y. State Herbarium. 

Rhytisma acerinum (Pers.) Fr.—Greenport on leaves of Acer rubrum. 

R. decolorans Fr.—Greenport on leaves of Xolisma ligustrina and Vaccinium. 

R. Solidaginis Schw.—On leaves of Solidago. 

R. Vitis Schw.—On leaves of grape; determined by Mrs. F. W. Patterson; speci- 
mens in N. Y. State Herbarium. 

Sarcoscypha occidentalis Schw. 

Sclerotinia fructigena (Pers.) Schroet.—On fruit of Amygdalus persica. 

S. Libertiana Fckl.—Determined at Bureau of Plant Industry. 

Tapesia fusca (Pers.) Fckl.—On oak. 


208 


ASCOMYCETES (PYRENOMYCETES) 


Botryosphaeria Berengeriana (DeNot.)—On twigs of Toxicodendron radicans. 

Calosphaeria Myricae (C. &. E) E. & E.—On dead Myrica carolinensis branches; 
reported in N. Y. State Mus. Bull. 167: 24. 1913. 

Coronophora angustata Fckl.—On dead Myrica carolinensis trunks; reported in 
N. Y. State Mus. Bull. 157: 24. I912. 

Daldinia concentrica (Bolt.) Ces. & DeNot.—On oak and hickory. 

D. vernicosa (Schw.) Ces. & DeNot.—On old wood of Fagus grandiflora. 

Diaporthe parasitica Murrill—On Castanea dentata. 

Diatrype albopruinosa (Schw.) Cke.—On Fagus grandiflora. 

D. stigma (Hoffm.) Fr.—On old wood of oak. 

Diatrypella betulina (Pk.) Sacc.—Greenport. 

D. prominens (Howe) E. & E.—On Platanus occidentalis. 

D. Rhois (Schw.) E. & E.—On Toxicodendron radicans. 

Dothidea Baccharidis Cke.—On dead branches of Baccharis halimifolia; determined 
by Mrs. F. W. Patterson; reported in N. Y. State Mus. Bull. 167: 26. I913. 

Eutypella clavulata Cke.—On dead branches of Ailanthus glandulosa. 

E. longirostris Pk.—On dead twigs of Robinia Pseudo-Acacia. 

E. stellulata (Fr.) Sacc.—On hickory, oak, Amelanchier and Robinia Pseudo-Acacia. 

Eutypa spinosa (Pers.) Tul.—On old wood of oak. 

Gloniopsis australis (Duby) Sacc.—Old wood of oak, Betula populifolia, Sassafras 
Sassafras and Vitis; specimens in N. Y. State Herbarium. 

Glonium parvulum (Ger.) Sace.—Decorticated wood; reported in N. Y. State Mus. 
Bull. 150: 45. i911. 

Herpotrichia diffusa (Fckl.) E. & E—On decaying wood of Robinia Pseudo-Acacia; 
reported in N. Y. State Mus. Bull. 150: 45. Ig1I. 

Hypoxylon atropunctatum (Fckl.) Cke-——On old wood of oak. 

H. coccineum Bull.—On old wood of oak and Malus Malus. 

H. fuscopurpureum (Schw.) Berk.—On old wood of hickory. 

H. fuscum (Pers.) Fr.—On old wood of Fagus grandiflora. 

H. Sassafras (Schw.) Berk.—On old wood of Sassafras Sassafras. 

H. serpens (Pers.) Fr.—Greenport on hickory and Quercus alba; specimens in N. Y. 
State Herbarium. 

Hysteriographium Mori (Schw.) Rehm—On old wood of oak, Platanus occidentalis, 
Malus Malus, Ligustrum vulgare and Baccharis halimifolia. 

Hysterium Thujarum Cke. & Pk.—Determined by Dr. F. J. Seaver. 

Hysterium pulicare Pers—On old wood of Robinia Pseudo-Acacia and Rhus; 
specimens in N. Y. State Herbarium. 

Massaria inquinans (Tode) Fr. 

M. vomitoria B. & C.—On Acer rubrum. 

Nectria cinnabavina (Tode) Fr.—Also the conidial form, Tubercularia vulgaris 
Tode on dead wood of many species of trees and shrubs. 

NN. episphaeria (Tode) Fr.—Parasitic on Diatrype stigma. 

Nummularia clypeus (Schw.) Cke.—On oak stump. 

N. discreta (Schw.) Tul.—On old branches of Malus Malus. 

Phyllachora graminis (Pers.) Fckl——On leaves of grasses. 

Plowrightia morbosa (Schw.) Sacc.—Branches of Prunus maritima and cultivated 
quince. 


209 


Rosellinia mutans (C. & P.) Sace.—On hickory; specimens in N. Y. State Her- 
barium. 

R. subiculala (Schw.) Sace.—Greenport on Fraxinus americana. 

Sphaerella Fragariae (Tul.) Sacc.—On leaves of Fragaria virginiana. 

Ustulina vulgaris Tul.—On oak stumps. 

Valsa ambiens (Pers.) Fr.—On dead branches of Fagus grandz/flora. 

V. Linderae Pk.—On dead twigs of Benzoin aestivale; specimens in N. Y. State 
Herbarium. 

V. rhoéphila C. & E.—On dead branches of Rhus; specimens in N. Y. State 
Herbarium. 

Xylaria polymorpha (Pers.) Grevy.—On hickory stump. 


HYPOMYCETES 


Aliernaria Brassicae (Berk.) Sacc.—On old plants of Ricinus communis and Brassica 
oleracea; determined at Cornell University. 

Cercospora leptosperma Pk.—On leaves of Aralia nudicaulis; determined by Dr. 
H. D. House. 

Illosporium roseum (Schreb.) Mart.—On Physcia stellaris. 

Macrosporium commune Rabenh.—On leaves of cucumber and watermelon. 

Microstroma Juglandis (Bereng.) Sacc.—On hickory leaves. 

Monilia Peckiana S. & V.—On leaves of Gaylussacia baccata; specimens in N. Y. 
State Herbarium. 

Oospora scabes Thaxt.—Common and very bad on potatoes. 

Ovularia obliqua (Cke.) Oud.—On leaves of Rumex. 

Pilacre faginea (Fr.) B. & Br. 

Piricularia grisea (Cke.) Sacc.—On leaves of Chaetochloa italica. 

Polythrincium Trifolit Kze.—On leaves of Trifolium pratense; determined by Dr. 
J. C. Arthur. 

Ramularia Armoraciae Fckl.—On leaves of Armoracia Armoracia. 

R. lineola Pk.—On leaves of Leontodon Taraxacum. 

R. Plantaginis E. & M.—The var. nigromaculans Pk., on leaves of Plantago major. 

Rhinotrichum ramosissimum B. & C.—On cherry limbs. 

Sireptothrix fusca Cda—On Juniperus virginiana; specimens in N. Y. State 
Herbarium. 


MELANCONIALES 


Coryneum pulvinatum K. & S.—On dead branches of Tilia americana. 

C. pustulatum Pk.—On dead branches of Castanea sativa; specimens in N. Y. State 
Herbarium. 

Gloeosporium intermedium brevipes Sacc.—On leaves of the cultivated rubber-plant. 
(Gloeosporium elasticae Cke. & Mass.) 

Pestalozzia adusta E. & E.—On leaves of Padus virginiana. 

P. funerea Desm.—On dead twigs of Juniperus virginiana. 

P. longiseta Speg.—On leaves of Rubus and Aronia. The three species of Pestalozzia 
are reported in N. Y. State Mus. Bull. 157: 30. tIg912. 

Steganosporium fenestratum (E. & E.) Sacc.—On dead branches of Clethra alnifolia; 
reported in N. Y. State Mus. Bull. 157: 34. tIg912. 


210 


SPHAEROPSIDEAE 


Amerosporium oeconomicum Ell. & Tracy—On bean leaves; determined by Mrs. 
F. W. Patterson. 

Ascochyta Rhei E. & E.—On leaves of Rheum rhaponticum; reported in N. Y. State 
Mus. Bull. 157: 22. Io12. 

Camarosporium abnorme (Pk.) Sacc.—On stems of Celastrus scandens. 

C. Maclurae Pk.—On dead branches of Toxylon pomiferum; Orient is the type 
station for this species; reported and described in N. Y. State Mus. Bull. 157: 
22 OTee 

Cytospora chrysosperma (Pers.) Fr.—On dead branches of poplar. 

C. Salicis (Cda.) Rabenh.—On dead willow branches; reported in N. Y. State Mus. 
Bull. 157: 25. 1912. 

Dendrophoma Tiliae Pk.—On Tilia americana; specimens in N. Y. State Her- 
barium. 

Diplodia ruborum (Schw.) Sacc.—On Rubus. 

D. virginiana Cke. & Rav.—On dead twigs of Juniperus virginiana. 

Hapflosporella Ribis Sacc.—On dead stems of Grossularia; reported in N. Y. State 
Mus. Bull. 157: 27. I912. 

Hendersonia Grossulariae Oud.—On dead and dying stems of Grossularia reclinata; 
reported in N. Y. State Mus. Bull. 157: 28. I912. 

H. pubentis Cke.—On dead stems of Sambucus canadensis. 

Macrophoma albifructa (Pk.) Berl. & Vogl—On dead maple twigs. 

M. Juniperina Pk.—On dead Juniperus virginiana twigs; Orient is the type station 
for this species; reported and described in N. Y. State Mus. Bull. 167: 28. 1913. 

Phlyctaena septorioides Sacc.—On dead stems of Phytolacca americana. 

Phoma ampelinum B. & C.—On grape leaves. 

P. Asclepiadea E. & E.—On stems of Asclepias syriaca; reported in N. Y. State 

Mus. Bull. 167: 30. 1913. 

. Baccharidis Brun.—On dead stems of Baccharis halimifolia. 

. corylina (Thuem.) Sacc.—On dead stems of Corylus. 

. herbarum West.—On dead stems of Lilium, Rheum rhaponticum and Solidago. 

. moricola Sacc.—On dead twigs of Morus. 

sambucina Sacc.—On dead twigs of Sambucus canadensis. 

. semiimmersa Sacc.—On dead branches of Crataegus; reported in N. Y. State 

Mus. Bull. 167: 30. 10913. 

Phoma Smilacis Boy. & Jacz.—On dead stems of Smilax rotundifolia; reported in 
N. Y. State Mus. Bull. 157: 32. 10912. 

Phyllosticta Betae Oud.—On leaves of beet. 


yt ty ty ty 


P. circumscissa Cke.—On leaves of Amygdalus persica. 

P. cruenta (Fr.) Kx.—On leaves of Vagnera racemosa; determined by Mrs. Patter- 
son. 

. Digitalis Bell.On leaves of Digitalis. 

. Iridis E. & M.—On leaves of Iris versicolor; determined by Mrs. Patterson. 

. Labruscae Thuem.—On leaves of Parthenocissus tricuspidata. 

. phomiformis Sacc.—On leaves of Quercus alba. 

. rhoicola E. & E.—On leaves of Toxicodendron radicans; reported in N. Y. State 
Mus. Bull. 167: 30. 1913. 

. Smilacis E. & M.—On leaves of Smilax rotundifolia; determined by Mrs. 
Patterson. 


oh las} ls} lef ss} 


as) 


211 


Septoria Dianthi Desm.—On leaves of Dianthus; reported in N. Y. State Mus. 
Ballas 7 33. LOL: 

S. Kalmiaecola (Schw.) B. & C.—Leaves of Kalmia latifolia at Greenport and East 

Marion. 

. Oenotherae West.—On leaves of Oenothera. 

. Polygonina Thuem.—On leaves of Persicaria. 

. Ribis Desm.—On leaves of Ribes vulgare. 

. Rubi West.—On leaves of Rubus. 

Sphaeropsis Malorum Pk.—On dead branches of Malus Malus. 

S. Peckii Sacc-—On dead twigs of Padus virginiana. (Sphaeropsis anomala Pk.) 

S. Persicae E. & B.—On dead branches of Amygdalus persica; specimens in N. Y. 
State Herbarium. 

S. Tiliacea Pk.—On dead branches of Tilia americana. 


AHHYNH 


BASIDIOMYCETES 
USTILAGINACEAE 


Cintractia Junci (Schw.) Trel.—On Juncus tenuis. 

Urocystis sorosporioides Koern.—On Thalictrum; determined by Dr. G. P. Clinton. 

Tolyposporium bullatum (Schroet.) Schroet.—Fruiting panicles of Echinochloa 
Crus-galli; determined at Bureau of Plant Industry. 

Ustilago anomala Kze.—On Tiniaria Convolvulus. 

U. Avenae (Pers.) Jens.—On panicles of Avena sativa. 

U. hypodytes (Schl.) Fr.—Probably on Agropyron; determined by Dr. Clinton, 
who says, ““an uncommon smut for this host.” 

U. Maydis (DC.) Cda.—On Indian corn. 

U. Tritici (Pers.) Jens.—On Triticum. 

U. utriculosa (Nees) Tul.—On Polygonum. 


MELAMPSORACEAE 


Melampsora arctica Rostr.—On leaves of Salix discolor; determined by Dr. J. C. 
Arthur,* who says, “the most southern collection known for this species.’’ 
(Uredo Rostrupiana Arth.) 

M. Bigelowii Thuem.—Greenport on willow leaves. 

Melampsoridium Betulae (Schum.) Arth—Determined by Dr. Arthur. 


COLEOSPORIACEAE 


Coleosporium Solidaginis (Schw.) Thuem.—On leaves of Aster and Solidago; 
determined in part by Dr. Arthur and Dr. F. D. Fromme. 


PUCCINIACEAE 


Aecidium Majanthae Schum.—Orient on leaves of Vagnera racemosa. 

A. Uvulariae Schw.—Orient on leaves of Uvularia sessilifolia. 

Gymnoconia interstitialis (Schlect.) Lagh.—Orient on leaves of cultivated and 
wild Rubi. : 

Gymnosporangium germinale (Schw.) Kern.—The summer stage, Roestelia auran- 
* Specimens determined by Dr. J. C. Arthur and Dr. F. D. Fromme are pre- 

served in the Herbarium of Dr. Arthur at Purdue University, Lafayette, Indiana. 

The authors are indebted to Dr. Arthur, who has read the manuscript of the 

Rusts, and who made valuable suggestions. 


G. 


212 


tiaca Pk., on leaves of Amelanchier, Crataegus and quince. (Gymnosporangium 
clavipes C. & P.) 

Juniperi-Virginianae Schw.—The summer stage, Roestelia pyrata (Schw.) 
Thaxt., on Malus Malus leaves; and the winter stage on Juniperus virginiana 
at Orient; specimens in N. Y. State Herbarium. (Gymnosporangium macropus 
Link.) 

nidus-avis Thaxt.—The summer stage on leaves of Amelanchier, determined by 
Dr. Arthur; and the winter stage on Juniperus virginiana at Orient. 


Kuehneola obtusa (Strauss) Arth.—On leaves of Potentilla canadensis; determined 


by both Dr. Arthur and Dr. Fromme. 


Puccinia Asparagi DC.—On Asparagus officinalis. 


ba} iat rel his} 


y 


IB, 


. Asteris Duby—On Aster novi-belgit; determined by Dr. Arthur. 

. Caricis-Asteris Arth—Determined by Dr. Fromme. 

. Caricis-Solidaginis Arth.—On Carex; determined by Dr. Arthur. 

. Cicutae Lasch.—On leaves of Cicuta maculata at Orient and Greenport; deter- 


mined by Dr. Arthur, who says this species has been previously collected in 
“three widely separated localities, Florida, Nova Scotia and Nevada.” 


. coronata Cda.—On leaves of Rhamnus cathartica and Nothoholcus lanatus; deter- 


mined by Dr. Arthur; also on leaves of Avena sativa. (Puccinia Rhamni (Pers.) 
Wettst.) 
Cyani (Schleich.) Pass.—On Centaurea cyanus; determined by Dr. Arthur. 


Puccinia Eleocharidis Arth.—On leaves of Eupatorium; determined by Dr. Arthur. 


Se} bis} Fae) ly 


yt 


as) le 


. graminis Pers.—On leaves of grasses; the aecia on leaves of Berberis vulgaris. 

. Grossulariae (Pers.) Lagerh.—On Carex virescens; determined by Dr. Arthur. 
. Heliantht Schw.—On leaves of Helianthus. 

. Hieracit (Schum.) Mart.—On leaves of Hieracium Gronovii; determined by Dr. 


Arthur. 
Malvacearum Mont.—Orient on leaves of Malva rotundifolia and Althaea rosea. 
Menthae Pers.—On leaves of Koellia; determined by Dr. Fromme. 


. obscura Schroet.—On Juncoides campestre; determined by Dr. Arthur. 
. orbicula Pk.—On leaves of Nabalus trifoliatus; determined by Dr. Arthur. 
. Peckii (DeToni) Kellerman—Orient on leaves of Oenothera; determined by 


Mrs. F. W. Patterson. 


. Pimpinellae (Strauss) Link—Orient on leaves of Washingtonia Claytont. 
. Pruni-spinosae Pers.—On leaves of Prunus avium and Padus virginiana; deter- 


mined by Dr. Arthur. (Tvanzschelia punctata (Pers.) Arth.) 


. Sambuci (Schw.) Arth.—On leaves of Carex crinita and C. lurida; determined 


by Dr. Arthur; also the aecia on leaves of Sambucus canadensis at Orient. 


. Seymouriana Arth.—The aecia on leaves of Asclepias pulchra and the telia on 


Spartina at Orient; determined by Dr. Arthur who says, “‘in west-central United 
States the aecia are found also on A pocynum and Cephalanthus.”’ 


. Sorghi Schw.—On leaves of sweet corn. 
. Taraxaci Plowr.—On leaves of Leontodon Taraxacum; determined by Dr. 


Arthur. 


. triticina Erikss——On various species of Triticum; determined in part by Dr. 


Arthur. (Puccinia Rubigo-vera (DC.) Wint.) 


. uniporula Orton—On Carex virescens; determined by Dr. Fromme. 
. Violae (Schum.) DC.—On leaves of Viola primulifolia at Greenport; deter- 


mined by Dr. Fromme. 


213 


Uromyces appendiculatus (Pers.) Fr.—On leaves of Strophostyles helvola; deter- 
mined by Dr. Arthur. (Nigredo appendiculata (Pers.) Arth.) 

U. Caladii (Schw-) Farl.—Greenport on leaves of Arisaema triphyllum and Peltandra 
virginica. 

U. Lilii Clinton—On leaves of Lilium; determined by Dr. Arthur. (Nzgredo 
Lilii (Clinton) Arth.) 

U. Limonii (DC.) Lev.—On leaves of Limonium carolinianum; determined by 
Dr. Arthur. 

U. Peckianus Farl.—Orient on Distichlis spicata. Doubtless the Aecidium atriplicis 
Shear, reported in N. Y. State Mus. Bull. 157: 21. 1912, on leaves of Atriplex 
hastata at Orient belongs here. Aecidium atriplicis is a rust which has only 
been reported on shrubby species of Atriplex in the arid regions of western 
United States. 

Uromyces Silphiit (Burrill) Arth.—On Juncus tenuis; determined by Dr. Fromme. 
(Nigredo Silphii (Burrill) Arth.) 

U. Spartinae Farl.—Orient on Spartina; determined by Dr. Arthur. 

U. Toxicodendri B. & R.—Orient on leaves of Toxicodendron radicans; determined 
in part by Dr. Arthur. (Pileolaria Toxicodendri (B. & R.) Arth.) 


TREMELLACEAE 
Exidia glandulosa (Bull.) Fr.—On old oak and trunks of other trees. 
Tremella aurantia Schw.—On bark of Juniperus virginiana. 
T. frondosa Fr.—On oak stumps. 


DACRYOMYCETACEAE 
Calocera cornea Fr. 
Dacryomyces stillatus Nees—On old pine logs. 
Guepinia spathularia (Schw.) Fr.—Growing from crevices of an old log. 


EXOBASIDIACEAE 
Exobasidium Vaccinii (Fckl.) Woron.—On fruit of Gaylussacia baccata. 


THELEPHORACEAE 

Aleurodiscus Oakesii (B. & C.) Cke.—On the bark of living trunks of Osirya vir- 
giniana. 

Corticium effuscatum C. & E.—On hickory. 

C. lacteum Fr.—On cherry and Rhus. 

C. roseolum Mass.—On hickory and Vaccinium. 

Craterellus cornucopioides (L.) Pers.—Greenport. 

Hymenochaete corrugata (Fr.) Lev.—On hickory. 

H. Curtisii (Berk.)—On Quercus alba and Padus virginiana. (Stereum Curtisti 
Berk.) 

H. rubiginosa (Schrad.) Lev.—On oak and Castanea sativa logs; specimens in N. Y. 
State Herbarium. 

H. tabacina (Sow.) Lev.—On hickory, Myrica carolinensis and cherry; specimens 
often resupinate. 

Peniophora cinerea (Fr.) Cke.—On dead branches of Betula populifolia, Padus 
virginiana and maple. 

Solenia fasciculata Pers.—On hickory. 

S. ochracea Hoffm.—On rotten wood of hickory; specimens in N. Y. State Her- 
barium. 


214 


Stereum acerinum Pers.—On hickory and maple. 

S. acerinum nivosum Ray.—On dead branches of Juniperus virginiana; specimens 
in N. Y. State Herbarium. 

S. complicatum Fr.—On old limbs. 

S. frustulosum (Pers.) Fr.—On oak stumps. 

. hirsutum (Willd.) Fr.—On hickory and Nyssa sylvatica. 

. ochraceo-flavum Schw.—On Amelanchier. 

purpureum Pers.—On hickory and Acer rubrum; sometimes resupinate. 

. sericeum Schw.—On oak, Myrica carolinensis and Nyssa sylvatica. 

. Spadiceum Fr.—On oak. 

. verstiforme B. & C.—On Hamamelis virginiana. 

. versicolor Fr.—On oak. 

Thelephora caryophyllea (Schaeff.) Pers.—In cedar woods. 

T. intybacea Pers.—Greenport in woods. 

T. palmata (Scop.) Fr.—The var. americana Pk. in woods. 

T. terrestris Ehrh.—In sandy soil. 


HHAHHAHHLY 


CLAVARIACEAE 


Clavaria amethystina Bull.—Greenport and Orient. 
C. aurea Schaeff. 

. boirvytis Pers.—Greenport and Orient. 

. cinerea Bull. 

. coralloides L.—Greenport. 

. cristata Pers.—Greenport. 

. formosa Pers. 

. fusiformis Sow. 

. mucida Pers.—Rotten oak logs on Gardiner’s Island. 
. muscoides L. 

C. pulchra Pk. 

Sparassis crispa (Wulf.) Fr.—Greenport in woods. 


DAAQAAA Ga © 


HYDNACEAE 


Hydnum aurantiacum (Batsch) A. & S. 

H. chrysocomum Underw.—On oak. 

Hi. farinaceum Pers.—On old hickory wood. 

. ochraceum Pers.—On cherry and Malus Malus; sometimes resupinate. 
. scrobiculatum Fr.—Greenport. 

. spongiosipes Pk.—In cedar woods. 

. subfuscum Pk. 

. velatum B. & C.—On hickory. 

Irpex ambiguus Pk.—On pine log. 


my yy 


. cinnamomeus Kr.—On oak, Fagus grandiflora and Vaccinium. 

. lacteus Fr.—On dead branches of Ilex verticillata. 

. mollis B. & C.—On cherry. 

. paradoxus (Schrad.) Fr.—On Padus virginiana. 

. sinuosus KFr.—On dead branches of Padus virginiana. 

. Tulipiferae Schw.—On hickory, oak, Malus Malus and Baccharis halimifolia. 
Phliebia radiata Fr. 


NN AN RN 


215 


POLYPORACEAE 
Boletus affinis Pk.—Sandy woods. 
. affinis maculosus Pk. 
. auriporus Pk. 
. Ballouii Pk.—Greenport; reported in N. Y. State Mus. Bull. 157: 22. Ig12. 
. castaneus Bull. 
. chrysenteron Fr. 
. felleus Bull. 
pallidus Frost 
rubropunctus Pk. 
. scabery Fr.—Greenport. 
. subglabripes Pk. 
. subvelutipes Pk.—Sandy soil. 
Daedalea confragosa rubescens (A. & S.) Pk.—On willow, Betula populifolia, Nyssa 


Hoa dbowneoa 


sylvatica and Fraxinus americana. (Trametes rubescens (A. & S.) Fr.) 

D. quercina (L.) Pers.—On oak and Padus virginiana. 

Daedalea unicolor (Bull.) Fr.—On hickory and oak. 

Favolus canadensis Klotsch.—On dead limbs of Fagus grandiflora. 

Fomes annosus Fr.—On Juniperus virginiana; specimens in N. Y. State Herbarium. 

F. applanatus (Pers.) Fr.—On hickory and cherry. 

F. carneus Nees—On Juniperus virginiana. 

F. rimosus Berk.—On Robinia Pseudo-Acacia; specimens in N. Y. State Herbarium. 

F. salicinus (Pers.) Fr.—On willow. 

Ganoderma pseudoboletus (Jacq.) Murrill—On oak. 

Gloeoporus conchoides Mont.—On hickory and oak. 

Merulius tremellosus Schrad.—On dead wood of cherry. 

M. Ulmi Pk.—On dead Myrica carolinensis; reported in N. Y. State Mus. Bull. 
USS Ales’) Tfonen, 

Polyporus betulinus (Bull.) Fr.—On Betula populifolia. 

P. brumalis (Pers.) Fr.—On oak. 

. caesius (Schrad.) Fr.—On Malus Malus. 

. chioneus Fr.—On oak and Padus virginiana. 

. cupulaeformis B. & C.—On Fagus grandiflora. 

. epileucus Fr.—On oak. 

. fumosus (Pers.) Fr. 

. giganteus (Pers.) Fr.—Specimens in N. Y. State Herbarium. 

. gilvus Schw.—On Fagus grandiflora, oak, cherry and Xolisma ligustrina (ab- 

normal specimens). 

P. hispidus (Bull.) Fr.—On living oak trees. 

P. Spraguei B. & C.—On oak. 

P. sulphureus (Bull.) Fr.—On stumps. 

Polystictus circinatus Fr.—Greenport. 

P. hirsutus Fr.—On hickory and oak. 

P. pergamenus Fr.—On oak, cherry and Fagus grandifiora. 

P. velutinus (Pers.) Fr.—On Xolisma ligustrina. 

P. versicolor (L.) Fr.—On hickory and oak. 

Poria attenuata Pk.—On hickory. 

P. contigua (Pers.) Fr.—On Robinia Pseudo-Acacia. 


Ine} las] tas} ‘eh Mast bef lng) 


216 


P. ferruginosa (Schrad.) Fr.—On Ilex verticillata. 

P. floccosa Fr.—On oak, Sassafras Sassafras, Malus Malus, Pouns virginiana and 
Acer rubrum. 

. inermis KE. & E.—On Ilex verticillata and Toxicodendron radicans; specimens in 
N. Y. State Herbarium. 

. nitida (Pers.) Fr.—On cherry. 

. reticulata (Pers.) Fr.—On Juniperus virginiana. 

. subacida Pk. 

. subacida vesiculosa (B. & C.) Pk.—Specimens in N. Y. State Herbarium. 

. vulgaris Fr.—On Juniperus virginiana. 

Strobilomyces strobilaceus (Scop.) Berk.—Sandy woods. 

Trametes cinnabarina (Jacq.) Fr.—On cherry. 

T. Pini (Brot.) Fr.—On pine; specimens in N. Y. State Herbarium. 

T. sepium Berk.—On willow, hickory and cherry. 

T. suaveolens (L..) Fr.—On willow. 


ae) 


ie} Hs} tas} The} tas) 


AGARICACEAE 


Agaricus abruptibulbus Pk.—In cedar woods. 
A. campester L. 

A. micromegethus Pk.—In sandy soil. 
A. Rodmani Pk. 

Amanita Frostiana Pk. 

. Frostiana pallidipes Pk. 

. glabriceps Pk. 

. muscaria L.—Cedar woods. 

. muscaria formosa (G. & R.) Fr. 

. phalloides Fr.—A gray variety. 

. verna Fr. 


>> SB Bp BD 


Amanitopsis strangulata (Fr.) Roze 

A. vaginata (Bull.) Roze 

A. vaginata livida (Pers.) Pk. 

Armillaria mellea Vahl 

A. nardosmia Ellis—Greenport. 

Cantharellus infundibuliformis (Scop.) Fr. 

C. minor Pk. 

Clitocybe brumalis Fr.—In cedar woods. 

C. clavipes (Pers.) Fr. 

C. dealbata Sow. 

C. odora (Bull.) Fr. 

C. pithyophila Fr.—Specimens in N. Y. State Herbarium. 

Clitopilus abortivus B. & C. 

C. albogriseus Pk. 

C. orcella (Bull.) Fr. 

Collybia dryophila (Bull.) Fr. 

C. platyphylla Fr. 

C. radicata (Relh.) Fr.—A form approaching var. pusilla Pk. 

C. tuberosa (Bull.) Fr.—On decaying Lactarius; specimens in N. Y. State Her- 
barium. 


217 


C. velutipes (Curt.) Fr. 

Coprinus micaceus (Bull.) Fr. 

C. plicatilis (Curt.) Fr. 

Cortinarius heliotropicus Pk.—Greenport. 

Entoloma Grayanum Pk. 

F. gubatum Fr. 

Hygrophorus chlorophanus Fr. 

H. laetus (Pers.) Fr.—Specimens in N. Y. State Herbarium. 

A. miniatus Fr. 

H. miniatus subluteus Pk.—Specimens in N. Y. State Herbarium, 

H. psittacinus (Schaeff.) Fr. 

H. sordidus Pk.—Greenport; reported in N. Y. State Mus. Bull. 157: 28. to912. 

Hypholoma appendiculatum (Bull.) Fr. 

H. incertum Pk. 

Hi. perplexum Pk. 

H. sublateritium (Schaeff.) Fr.—Growing in clusters about stumps of hickory and 
oak. 

Laccaria amethystina (Bolt.) B. & Br. (in part)—Oak woods. 

L. laccata (Scop.) B. & Br. 

L. trullisata (Ellis) Pk.—In clean sand. (Clitocybe trullisata Ellis.) 

Lactarius Peckii Burl. 

. biperatus (Scop.) Fr. 

. serifluus (DC.) Fr. 

. subdulcis (Bull.) Fr. 

. theiogalus (Bull.) Fr. 

. vellereus Fr. 

. volemus Fr. 


HANAN 


Lentinus tigrinus (Bull.) Fr.—On dead trees; the diseased form which is known 
as Lentodium squamulosum Morg. 

Lenzites betulina (L.) Fr.—On oak; specimens in N. Y. State Herbarium. 

L. sepiaria Fr.—On pine (poroid form), Juniperus virginiana, Picea mariana and 
cherry; specimens in N. Y. State Herbarium. 

L. trabea (Pers.) Fr.—On pine; reported in N. Y. State Mus. Bull. 167: 27. 1913. 

Lepiota americana Pk. 

L. clypeolaria (Bull.) Fr. 

L. naucinoides Pk.—Cultivated fields. 

Marasmius androsaceus (L.) Fr. 

biformis Pk.—Swampy places. 

capillaris Morg.—On grass stems. 

elongatipes Pk. 

epiphyllus Fr.—On old leaves; reported in N. Y. State Mus. Bull. 157: 28. 

IQI2. 

insititius Fr.—On leaves and twigs. 

oreades Fr. 

ramulinus Pk.—On branches in cedar woods. 

salignus Pk.—On leaves and twigs. 

salignus major Pk. 

spongiosus B. & C.—Specimens in N. Y. State Herbarium. 


218 


M. subnudus (Ellis) Pk. 
M. velutipes B. & C.—On leaves. 
Mycena atroalboides Pk. 
M. corticola (Schum.) Fr.—On bark of Robinia Pseudo-Acacia and grape vines- 
M. epiptergyria (Scop.) Fr. 
M. galericulata (Scop.) Fr.—On logs. 
M. sanguinolenta (A. & S.) Fr.—Specimens in N. Y. State Herbarium. 
Omphalia campanella (Batsch) Fr.—On decaying coniferous wood and moss. 
Panaeolus papilionaceus Fr. 
P. retirugis Fr.—Cultivated fields. 
P. semiglobatus Murrill—Determined by Dr. W. A. Murrill. 
Panus rudis Fr.—On old oak wood. 
P. stypticus (Bull.) Fr.—On oak and Amygdalus persica stumps. 
P. torulosus Fr.—On Baccharis halimifolia. 
Pholiota praecox (Pers.) Fr. 
Pleurotus ostreatus (Jacq.) Fr.—On old poplar logs. 
P. septicus Fr. 
Pluteus cervinus (Schaeff.) Fr. 
Psathyrella disseminata (Pers.) Fr. 
Russula compacta Frost 
R. emetica Fr. 
R. foetens (Pers.) Fr.—Southold. 
R. foetentula Pk.—Southold. 
R. Mariae Pk. 
R. obscura Rom.—Greenport. 
R. pectinatoides Pk. 
R. purpurina Q. & S.—Orient and Greenport; specimens in N. Y. State Herbarium. 
R. virescens (Schaeff.) Fr.—Greenport and Orient. 
Schizophyllum commune Fr.—On hickory, cherry, Castanea sativa and Baccharis 
halimifolia. 
Stropharia aeruginosa (Curt.) Fr—On decaying wood. 
S. semiglobata (Bastch) Fr.—On horse manure. 
Tricholoma alboflavidum Pk. 
T. personatum Fr.—In oak woods. 
T. piperatum Pk.—Reported in N. Y. State Mus. Bull. 167: 32. 1913. 
T. resplendens Fr. 
T. Russula (Schaeff.) Fr. 
T. sejunctum Sow. 
Trogia crispa (Pers.) Fr.—On oak. 


GASTEROMYCETES ~ 


Anthurus borealis Burt—Orient in corn fields. 

Bovista pila B. & C.—In woods and fields. 

B. plumbea Pers. 

Calvatia craniiformis (Schw.) Morg.—In cedar woods; reported in N. Y. State 
Mus. Bull. 150: 24. Ig1t. 

C. cyathiformis (Bosc) Morg. 

C. rubroflava (Cragin )Morg.—Sandy soil; reported in N. Y. State Mus. Bull. 167: 
Di eeLOnae 


219 


Crucibulum vulgare Tul.—On hickory. 

Cyathus stercoreus (Schw.) DeToni 

C. vernicosus (Bull.) DC.—Sandy soil. 

Geaster hygrometricus Pers. 

G. minimus Schw.—Cedar woods. 

Lycoperdon atropurpureum Vitt. 

L. cruciatum Rostk.—In cultivated fields and open woods. 

L. echinatum Pers.—Greenport. 

L. pusillum Batsch 

L. pyriforme Schaeff.—On decayed cherry logs. 

L. Wrightit B. & C.—Greenport. 

Phallus impudicus L. 

Polysaccum pisocarpium Fr.—Southold and Orient on the ground in woods; re- 
ported in N. Y. State Mus. Bull. 157: 32. 1912. 

Scleroderma flavidum E. & E.—In cedar woods; specimens in N. Y. State Her- 
barium. © 

S. Geaster Fr.—In sandy soil; specimens in N. Y. State Herbarium. 

SS. tenerum B. & C.—In cedar woods. 

LS. verrucosum (Bull.) Pers.—Greenport. 

S. vulgare Hornem.—In cedar woods; specimens in N. Y. State Herbarium. 


LICHENES 


Arthonia lecideella Nyl.—On 1 = of Tilia americana; determined by Dr. Bruce 
Fink. 

A. quintarvia Nyl.—On A’ nithus glandulosa and Rhus bark; determined by G. K. 
Merrill; reported in N. Y. State Mus. Bull. 167: 23. 1913. 

A. radiata (Pers.) Th. Fr.—On hickory, Fagus grandiflora, Amelanchier, Acer rubrum 
and Tilia americana bark. (Arthonia astroidea Ach.) 

Baeomyces roseus Pers.—East Marion on earth in woods. 

Biatora flecuosa Fr.—Dead limbs of Juniperus virginiana; determined by Dr. H. E. 
Hasse.* 

B. varians (Ach.) Tuck.—Determined by Dr. Hasse. 

B. vernalis (L.) Fr.—On cedar fence rails; determined by Dr. Hasse. 

Biatora (§ Biatorina) cyrtella (Ach., Nyl.) Tuck.—Determined by Dr. Hasse. 

Biatora (§ Bacidia) rubella (Ehrh.) Rabenh.—On bark of Juniperus virginiana and 
Toxicodendron radicans; determined by Dr. L. W. Riddle. 

B. (§ Bacidia) Schweinitzii Fr.—On Juniperus virginiana; determined by Dr. 
Hasse. 

Biatora (§ Biatorella) simplex (Dayv.)—On rocks; determined by Dr. Hasse. 

Cetraria Islandica (L.) Ach.—Partly determined by Dr. Hasse. 

-Cladonia alpestris (L.) Rabenh. 

-C. bacillaris clavata (Ach.) Wainio—On pine bark and Juniperus virginiana stumps. 

C. Boryi Tuck., forma reticulata (Russell) Merrill—Specimens in N. Y. State Her- 
barium. 

C. caespiticia (Pers.) Flk.—Sandy soil at East Marion. 

-C. cariosa cribosa (Wallr.) Wainio—On earth. 

C. cristatella Tuck.—On old coniferous logs. 
* Specimens of the Lichens named by Dr. Hasse are preserved in the Lichen 

Herbarium of The Sullivant Moss Society. 


220 


C. cristatella ochrocarpia Tuck.—Determined by Dr. Hasse. 

C. cristatella vestita Tuck.—Greenport; reported in N. Y. State Mus. Bull. 167: 34. 
1913. 

C. digitata (Ach.) Schaer.—Light soil in open woods at Orient and East Marion; 
determined by Dr. Hasse. 

C. digitata ceruchoides Wainio—Determined by Dr. Hasse. 

Cladonia fimbriata radiata (Schreb.) Fr.—Sandy soil; determined by Dr. Hasse. 

C. furcata (Huds.) Schrad.—On earth. 

C. furcata pinnata (Flk.) Wainio, f. foliolosa Del.—Determined by Dr. Hasse. 

C. furcata racemosa (Hoffm.) Flk.—Determined by Dr. Hasse. 

C. gracilis dilatata (Hoffm.) Wainio—Sandy soil; determined by Dr. Riddle; 
reported in N. Y. State Mus. Bull. 167: 34. I913. 

C. macilenta (Ehrh.) Hoffm.—A composite species on coniferous wood; partly 
determined by Dr. Hasse. 

C. mitrula Tuck. 

C. pyxidata chlorophaea (Spreng.) Flk.—Determined by Dr. Hasse. 

C. pyxidata neglecta (Flk.) Mass.—On limbs of Juniperus virginiana and on earth. 

C. pyxidata neglecta, m. lophyra Ach.—Determined by Dr. Hasse. 

C. rangiferina (L.) Weber 

C. squamosa (Scop.) Hoffm.—A variety of this composite species; determined by 
Dr. Hasse. 

C. sylvatica (L.) Rabenh. 

C. turgida conspicua (Schaer.) Nyl.—Determined by Dr. Hasse. 

C. uncialis (L.) Fr.—A variety of this composite species. 

C. verticillata Hoffm. 

Collema (§ Synechoblastus) nigrescens (Huds.) Ach.—On Juniperus virginiana trees ; 
determined by Dr. Hasse. 

Graphis dendritica Ach., f. obtusa Leight.—On bark of Acer rubrum; determined 
by Dr. Hasse. 

G. scripta (L.) Ach.—On hickory, oak and Fagus grandiflora bark. 

G. scripta recta (Humb.) Koerb.—Determined by Dr. Hasse. 

G. scripta serpentina (Ach.) Nyl.—Determined by Dr. Hasse. 

Lecanora (§ Candelaria) laciniosa (Duf.) Nyl.—On Juniperus virginiana and 
Nyssa sylvatica; also old leather. (Teloschistes concolor (Dicks.) Tuck.) 

L. (§ Candelaria) laciniosa effuse (Tuck.) n. comb.—Reported in N. Y. State Mus. 
Bull. 150: 49. IgtT. 

Lecanora (§ Callopisma) camptidia (Tuck.) Nyl——On oak bark at Orient; deter- 
mined by Dr. Riddle; reported in N. Y. State Mus. Bull. 167: 30. 1913. 
(Placodium camptidium Tuck.) 

L. (§ Callopisma) cerina (Ehrh.) Ach.—On Juniperus virginiana; determined by 
Dr. Fink; specimens in N. Y. State Herbarium. 

Lecanora (§ Callopisma) ferruginea discolor (Willey) n. comb.—On Juniperus 
virginiana; determined by Dr. Fink; reported in N. Y. State Mus. Bull. t50: 
2 Onis 

L. (§ Callopisma) ferruginea nigricans (Tuck.) Nyl.—Determined by Dr. Hasse. 

Lecanora (§ Rinodina) ascociscana (Tuck.) Nyl.—Bark of trees; determined by Dr. 
Hasse. 

L. (§ Rinodina) exigua (Ach.) Th. Fr.—Determined by Dr. Hasse. 


221 


L. (§ Rinodina) sophodes (Ach.) Koerb.—On bark of Baccharis halimifolia; deter- 
mined by Dr. Riddle. 

Lecanora Hageni Ach.—Determined by Dr. Hasse. 

L. pallida (Schreb.) Tuck.—On bark of Ilex verticillata. 

L. pallida cancriformis (Hoffm.) Tuck.—On bark of oak and Amelanchier; deter- 
mined by both Dr. Fink and Dr. Riddle. 

L. subfusca (L., Nyl.) Ach.—On bark of oak, Juniperus virginiana and Robinia 
Pseudo-Acacia; partly determined by Dr. Fink. 

L. subfusca allophana Ach.—On limbs of Juniperus virginiana; determined by Dr. 

Riddle; specimens in N. Y. State Herbarium. 

. subfusca rugosa (Pers.) Cromb.—Determined by Dr. Hasse. 

. symmictera Nyl.—Determined by Dr. Hasse. 

. varia (Ehrh.) Ach.—On bark of Juniperus virginiana and Pyrus communis. 

. varia saepincola Fr.—On old chestnut fence post; reported in N. Y. State Mus. 

Bull. 150: 46. Io1t. 

Lecanora (§ Aspicilia) cinerea (L.) Sommf.—On rocks. 

Lecanora (§ Acarospora) cervina squamulosa Fr.—Determined by Dr. Hasse. 

L. (§ Acarospora) fuscata (Schrad.) Fr.—On rocks; determined by Dr. Hasse. 

Lecidea (§ Buellia) disciformis (Fr.) Nyl—On oak, Amygdalus persica, Robinia 
Pseudo-Acacia and Sambucus canadensis bark; Greenport on bark of Fagus 
grandiflora; partly determined by Dr. Hasse. 

L. (§ Buellia) myriocarpa (DC.) Nyl.—On pine, Juniperus virginiana and Rhus 
bark; partly determined by Dr. Fink, also Dr. Hasse; specimens in N. Y. 


ISU st tet les 


State Herbarium. 

Lecidea albocaerulescens (Wulf.) Schaer.—Determined by Dr. Hasse. 

Leptogium tremelloides (L. f.) S. F. Gray—On Juniperus virginiana. 

Myriangium Duriaei (Mont. & Berk.) Tuck.—On bark of Fraxinus americana at 
East Marion; determined by Dr. Hasse. 

Opegrapha herpetica Ach.—On bark of Tilia americana; determined by Mr. Merrill; 
reported in N. Y. State Mus. Bull. 167: 29. 1913. 

O. varia Pers.—On bark of hickory, Ailanthus glandulosa and Tilia americana; in 
part determined by Dr. Riddle. 

O. varia pulicaris (Ach.) Nyl.—Determined by Dr. Hasse. 

Opegrapha vulgata Ach.—Determined by Dr. Hasse. 

Pannaria luridum (Mont.) Nyl.—Rare at Orient on bark of Juniperus virginiana; 
determined by Dr. Fink; specimens in N. Y. State Herbarium. (Physma 
luridum (Mont.) Tuck.) 

Parmelia caperata (L.) Ach.—On Juniperus virginiana. 

P. colpodes Ach.—Rare at Orient; specimens in N. Y. State Herbarium. 

P. conspersa (Ehrh.) Ach.—On rocks. 

-P. crinita pilosella (Hue) Merrill—On Juniperus virginiana. 

P. dubia (Wulf.) Schaer.—On trunks of oak. (Parmelia Borreri Tuck.) 

P. dubia hypomela (Tuck.) n. comb.—On Juniperus virginiana; reported in N. Y. 

State Mus. Bull. 150: 47. Ig1t. 

. exasperata (Ach.) DN.—Determined by Dr. Hasse. (Parmelia olivacea aspidota 

Ach.) : 

. hyperopta Ach.—Determined by Dr. Hasse. 
. olivacea (L.) Ach.—On oak bark. 


ae) 


Se} tas! 


222 


P. perforata (Jacq.) Ach.—On oak; specimens in N. Y. State Herbarium. 

P. perforata hypotropa (Nyl.) Tuck.—On Juniperus virginiana; determined by Dr. 
Fink; reported in N. Y. State Mus. Bull. 150: 47. Ig11. : 

P. vudecta Ach.—On Juniperus virginiana; specimens in N. Y. State Herbarium. 
(Parmelia Borreri rudecta (Ach.) Tuck.) 

P. saxatilis (L.) Fr.—On rocks. 

P. sulcata Tayl.Specimens in N. Y. State Herbarium. (Parmelia saxatilis 
sulcata Nyl.) 

P. tiliacea Ach.—On trunks of Malus Malus. 

Peltigera canina (L.) Hoffm.—On earth; determined by Dr. Hasse. 

Pertusaria communis Lam. & DC.—On hickory, oak and Fagus grandiflora; deter- 
mined by both Dr. Fink and Mr. Merrill. 

P. leioplaca (Ach.) Schaer.—On Quercus velutina; determined by Mr. Merrill; 
specimens in N. Y. State Herbarium. 

P. multipuncta (Turn.) Nyl.—On hickory; in part determined by Dr. Hasse. 

P. pustulata (Ach.) Nyl.—Orient and Greenport on Myrica carolinensis; deter- 
mined by Mr. Merrill. 

P. velata (Turn.) Nyl.—Determined by Dr. Fink. 

P. Wulfenit Lam. & DC.—On oak at East Marion; determined by Dr. Hasse. 

Physcia (§ Xanthoria) parietina (L.) DN.—Determined by Dr. Hasse. (Telo- 
schistes parietinus (L.) Norm.). 

P. (§ Xanthoria )parietina aureola (Ach.) Nyl.—On Robinia Pseudo-Acacia; deter- 
mined by Dr. Hasse. 

P. (§ Xanthoria) polycarpa (Ehrh.) Nyl.—Determined by Dr. Hasse. 

Physcia (§ Pseudophyscia) hypoleuca (Muhl.) Tuck.—Rare at Orient on Juniperus 
virginiana bark; determined by Miss Mary F. Miller; specimens in N. Y. State 
Herbarium. 

P. (§ Pseudophyscia) speciosa (Wulf.) Nyl.—Determined by Dr. Hasse. 

Physcia hispida (Schreb.) Tuck.—Orient, very rare on a Juniperus virginiana 
stump; determined by Dr. Fink; reported in N. Y. State Mus. Bull. 150: 36. 
IQIt. 

P. obscura (Ehrh.) Nyl—On bark of Juniperus virginiana; determined by Dr. 
Hasse. 

P. obscura endochrysea (Hampe) Nyl.—On Juniperus virginiana. 

P. stellaris (L.). Nyl—On Juniperus virginiana; specimens in N. Y. State Her- 
barium. 

P. tribacia (Ach.) Nyl.—On Juniperus virginiana and Robinia Pseudo-Acacia; also 
on rocks. 

Platysma aurescens (Tuck.) Nyl—Determined by Dr. Hasse. (Cetraria aurescens 

Tuck.) 

. ciliare (Ach.) Nyl. 

. Fendlerit (Tuck.) Nyl.—Determined by Dr. Hasse. 

. glaucum (L.) Nyl.—Determined by Dr. Hasse. 

. lacunosum (Ach.) Nyl. 

Pyrenula nitida Ach.—Greenport on trunks of Fagus grandiflora. 

Pyxine sorediata (Ach.) Fr.—On oak, Juniperus virginiana and Robinia Pseudo- 
Acacia bark. 

Ramalina calicaris (L.) Nyl.—On Juniperus virginiana; in part determined by Dr. 


as} fash tas} las} 


Hasse. 


223 


R. calicaris subampliata Nyl.—On Juniperus virginiana; reported in N. Y. State 
Mus. Bull. 150: 47. I9tI, as Ramalina calicaris fraxinea Fr. 

R. subfastigiata Nyl.—On oak, Juniperus virginiana and Robinia Pseudo-Acacia; 
determined by Dr. Hasse. 

R. tenuis Tuck., Merrill—On Juniperus virginiana; reported in N. Y. State Mus. 
Bull. 150: 38. r911, as Ramalina rigida (Pers.) Ach. 

Sagedia cestrensis Tuck.—Orient on bark of hickory and Tilia americana; deter- 
mined by Miss Miller; reported in N. Y. State Mus. Bull. 157: 33. 1912. 

Teloschistes chrysopthalmus (L.) Th. Fr.—Determined by Dr. Hasse, who says, “‘an 
unusual form on account of almost entire absence of fibrillae.”’ 

T. flavicans (Sw.) Norm.—Orient on Juniperus virginiana; determined by Dr. Fink; 
reported in N. Y. State Mus. Bull. 150: 39. tIo1ItI. 

Usnea ceratina Ach.—Determined by Dr. Hasse, who says, ‘“‘the color of the 
thallus is unusually dark.”’ 

U. florida (L.) Hoffm.—On pine and Juniperus virginiana; determined by Dr. 
Hasse. 

U. florida rubiginea Mx.—On Juniperus virginiana. 

U. hirta (L.) Hoffm. 

U. trichodea Ach.—On Juniperus virginiana; reported in N. Y. State Mus. Bull. 
I50: 40. IoQtIt. 

Xylographa parallela (Ach.) Fr.—Determined by Dr. Hasse. 


HEPATICAE 
Anthoceros laevis L. 


Calypogeia Sullivanti Aust.—Determined by G. B. Kaiser. 

C. Trichomanis (L.) Cda.—Determined by Miss Annie Lorenz. 

Cephalozia curvifolia (Dicks.) Dumort.—On an old log in wet woods at Greenport; 
determined by Dr. G. B. Conklin. 

Frullania Asagrayana Mont.—On a rock in swampy woods; determined by both 
Dr. Conklin and Mr. Kaiser. 

F. eboracensis Gottsche—On bark of Juniperus virginiana. 

Lophocolea heterophylla (Schrad.) Dumort.—Determined by Dr. Conklin. 

Marchantia polymorpha L.—Determined by Dr. Conklin. 

Odontoschisma prostratum (Sw.) Trev.—Determined by Miss Lorenz; specimens in 
N. Y. State Herbarium. 

Pellia epiphylla (L.) Cda.—On earth. 

Porella pinnata L.—Trunks of bushes in swamps; determined by Mr. Kaiser. 

P. platyphylla (L.) Lindb.—Trunks of trees. 

Ptilidium pulcherrimum (Web.) Hampe 

Radula complanata (L.) Dumort. 

Ricciella fluitans (L.) A. Br.—On mud in a pond; determined by Mr. Kaiser. 

Riccia Sullivantit (Aiist.) Evans. 

Ricciocarpus natans (L.) Cda.—Floating in water. 


Musc1r 


Amblystegium riparium B. & S.—In swamps. 

A. riparium longifolium (Schultz) B. & S—Determined by G. B. Kaiser.* 

A. serpens (L.) B. & S. 

Anomodon atienuatus (Schreb.) Hueb.—About base of trees in woods at Greenport; 
determined by Mr. Kaiser. 


224 


A. rostratus (Hedw.) Schimp.—Determined by Mr. Kaiser. 

Aulacomnium palustre (L.) Schwaegr.—In swamps. 

Brachythecium oxycladon (Brid.) J. & S.—On trunks of trees. 

B. rivulare B. & S.—Wet places. 

B. rutabulum (L.) B. & S.—Sandy soil. 

B. velutinum (L.) B. & S.—On soil at base of trees. 

Bryhnia Novae-Angliae (S. & L.) Grout—Swamps at Greenport. 

Bryum caespiticium L.—Greenport; determined by Dr. A. W. Evans. 

Campylium hispidulum (Brid.) Mitt.—Determined by Mr. Kaiser. 

C. radicale (Bv.) Grout—Determined by Mr. Kaiser. 

Catharinea angustata Brid.—Shaded sandy soil. 

C. undulata (L.) W. & M. 

Ceratodon pur pureus (L.) Brid.—Sandy soil. 

Climacium Kindbergii (R. & C.) Grout—On roots of trees in wet places; reported 
in N. Y. State Mus. Bull. 150: 25. I91I. 

Dichelyma capillaceum B. & S.—On Cephalanthus occidentalis in a swamp. 

Dicranella heteromalla (L.) Schimp. 

Dicranum Drummondii CM.—Wet woods at Greenport; determined by Mr. 
Kaiser. 

D. flagellare Hedw. 

D. fuluum Hook.—Determined by Mr. Kaiser. 

D. pallidum B. & S.—Sandy beach in open cedar woods; determined by Mr. 
Kaiser. 

D. scoparium (L.) Hedw. 

Ditrichum pallidum (Schreb.) Hampe—In cedar woods. 

Drepanocladus aduncus gracilescens (Schimp.)—In swamps. 

D. fluitans (Dill.) Warnst.—East Marion. 

Entodon seductrix (Hedw.) CM.—Wet log in a swamp; determined by Mr. Kaiser 

Eurhynchium hians (Hedw.) J. & S.—Sandy soil. 

E. serrulatum (Hedw.) Kindb.—Determined by Mr. Kaiser. 

E. strigosum (Hoffm.) B. & S. 

Fontinalis Sullivantit Lindb.—Greenport on roots and trunks of bushes in a swamp; 
determined by Mr. Kaiser. 

Funaria flavicans Mx. ; 

F. hygrometrica (L.) Sibth.—Greenport; determined by Dr. Evans. 

Hedwigia albicans (Web.) Lindb.—Base of oak trees. 

Hypnum cupressiforme L.—Determined by Mr. Kaiser. 

H. cupressiforme resupinatum (Wils.) Schimp.—Determined by Mr. Kaiser. 

H. curvifolium Hedw. 

H. Haldanianum Grev.—On old logs and stumps; in part determined by Mr. 

Kaiser. 

. imponens Hedw.—Moist places. 

. Patientiae Lindb.—Determined by Mr. Kaiser. 

. recurvans (Mx.) Schwaegr.—On moist earth; determined by Mr. Kaiser. 

. reptile Mx.—Greenport in moist woods; determined by Mr. Kaiser. 

Leptobryum pyriforme (L.) Wils. 


Teese 


* Specimens of the Mosses named by G. B. Kaiser are preserved in the Moss 
Herbarium of The Sullivant Moss Society. 


225 


Leucobryum glaucum (L.) Schimp. 

Leucodon brachypus Brid.—On bark of Juniperus virginiana; determined by Mr. 
Kaiser. 

L. julaceus (Hedw.) Sull.—On Juniperus virginiana bark. 

Mniobryum albicans (Wahl.) Limpr.—Determined by Mr. Kaiser. 

Mnium affine ciliare (Grev.) CM.—Wet places. 

M. cuspidatum (L.) Leyss—On rotten logs and moist soil; in part determined by 
Mr. Kaiser. 

M. hornum L.—Edge of a swamp. 

M. rostratum Schrad. 

Orthotrichum strangulatum Sull.—Greenport on trees; determined by Mr. Kaiser. 

Physcomitrium turbinatum (Mx.) Brid.—Greenport; determined by Dr. Evans. 

Plagiothecium denticulatum (L.) B. & S.—Wet places at Greenport. ~ 

P. Ruthei Limpr.—Determined by Mr. Kaiser. 

P. striatellum (Brid.) Lindb.—Greenport in moist soil; determined by Mr. Kaiser. 

P. sylvaticum (Huds.) B. & S.—Sandy soil; determined by Mr. Kaiser. 

P. turfaceum Lindb.—On stumps of Juniperus virginiana. 

Pleuridium subulatum (L.) Rabenh.—Determined by Mr. Kaiser. 

Pogonatum brachyphyllum (Mx.) Bv.—Orient; determined by G. B. Nichols. 

Pohlia nutans (Schreb.) Lindb.—Greenpert in light soil in woods; also on sandy 
beach at Orient; determined by Mr. Kaiser. 

Polytrichum commune L.—Dry woods. 

P. juniperinum Willd.—Determined by G. B. Kaiser. 

P. Ohioense B. & C.—Wet woods at Greenport; determined by Mr. Kaiser. 

P. piliferum Schreb. 

Pylaisia Schimperi R. & C. 

Sphagnum acutifolium Ehrh.—Determined at Bureau of Plant Industry. 

S. cuspidatum Ehrh.—Wet open meadow; determined by Mr. Kaiser. 

S. cymbifolium Ehrh.—Determined at Bureau of Plant Industry. 

S. recurvum By.—Determined at Bureau of Plant Industry. 

S. Torreyanum Sull.—Boggy woods at Greenport; determined by Mr. Kaiser. 

Thelia hirtella (Hedw.) Sull.—Base of oak and other trees. 

T. Lescurit Sull.—Sandy soil; determined by Mr. Kaiser. 

Thuidium delicatulum (L.) Mitt. 

T. paludosum (Sull.) Rau & Herv.—Wet open soil; determined by Mr. Kaiser. 

T. scitum (Bv.) Aust.—Base of oak trees; determined by Mr. Kaiser. 

Tortella caespitosa (Schwaegr.) Limp:s.—Sandy beach; determined by Mr. Kaiser. 

Ulota americana (Bv.) Lindb.—Rocks. 

U. crispa Brid.—Bark of an old oak; determined by Mr. Kaiser. 

Webera sessilis (Schmid.) Lindb.—On rich banks at Greenport. 

Weisia viridula (L.) Hedw.—Sandy soil. 


(To be continued.) 


226 


REVIEWS 


The Salton Sea* 


The flooding of Salton Sink, in 1907, was the beginning of a 
problem that offered many attractions to botanists and a history 
of those investigations is contained in the volume now issued by 
the Carnegie Institution. The breaking of the banks of the 
Colorado and the consequent flooding of a region of about 450 
square miles, the final control of the river and the gradual 
recession of the water by evaporation has made a condition 
that is perhaps unique in the world. Dr. MacDougal was quick 
to detect the unrivalled opportunity to study the revegetation of 
the banks of a slowly drying inland sea, and the thoroughness 
with which the undertaking has been carried on is evidenced 
by the list of articles in the accompanying footnote. 

From the purely ecological and phytogeographical standpoint 
the contributions of Dr. Parish and Dr. MacDougal are the most 
interesting, but their work necessarily rests on the foundation 
erected by the other contributors to the volume. The descrip- 
tion of the revegetation of the beaches, caused by the gradual 
drying up of the sea (nearly 10 square miles annually was thus 
added), and the discussion of the factors that played their part 
in the process, are the chief contributions of the volume. There 
are bound up with such studies great problems of general bearing, 
dealing with the behavior of plants under new and constantly 


* MacDougal, D. T. and collaborators. The Salton Sea, a study of the 
geography, the geology, the floristics and the ecology of a desert basin. 182 pp. + 
32 plates + 4 figures in the text. Carnegie Institution of Washington Publicaticn 
No. 193. 30 June, 1914. Containing: The Cahuilla Basin and desert of the 
Colorado, by W. P. Blake, pp. 1-12; Geographical features of the Cahuilla 
Basin, by G. Sykes, pp. 13-20; Sketch of the geology and soils of the 
Cahuilla Basin, by E. E. Free, pp. 21-33; Chemical Composition of the water of 
Salton Sea and its annual variation in concentration 1906-1911, by W. H. Ross, 
pp. 35-46; Variations in composition and concentration of water of Salton Sea, 
1912 and 1913, by A. E. Vinson, pp. 47-48; Behavior of certain micro-organisms in 
brine, by G. J. Pierce, pp. 49-70; Action of Salton Sea water on Vegetable Tissue, 
by M. A. Brannon, pp. 71-78; The tufa deposits of the Salton Sink, by J. C. Jones, 
pp. 79-84; Plant ecology and floristics of Salton Sink, by S. B. Parish, pp. 85-114; 
Movements of vegetation due to submersion and desiccation of land areas in Salton 
Sink, and a General Discussion, both by D. T. MacDougal, pp. 115-182. 


227 


changing environmental conditions, and the effect of this be- 
havior on the movement and association of species. From this 
standpoint the book is a notable addition to the literature of 
botany. Some, perhaps too carping, systematic botanists may 
quarrel with the publication of a new name for a species of 
Chamaesyce, without description, simply saying ined. n.sp. (p. 
110). There has been, too, some carelessness in proof-reading, 
such as Geranaceae for Geraniaceae (p. 109) and Asclepiaceae for 
Asclepiadaceae (p. 175). But such trivial matters are lost sight 
of in the fact that the volume is a really splendid contribution 
to botanical literature. 

The illustrations and maps are very fine, in many cases showing 
beautiful views of the region. The failure of the publication to 
contain an index must reduce its usefulness to many. 

Noe: 


NEWS ITEMS 


Dr. Arthur Harmount Graves has resigned his position as As- 
sistant Professor of Botany in the Sheffield Scientific School of 
Yale University, and is at present engaged in research at the 
laboratory of Professor V. H. Blackman, Professor of Plant 
Physiology and Pathology, Royal College of Science, South 
Kensington, London, England. Dr. Graves has been a member 
of the faculty of Yale for the past twelve years. 


The Long Island Historical Society has recently deposited with 
the Brooklyn Botanic Garden the herbarium of the Society. It 
consists of a general herbarium and a special collection of Long 


Island plants, many of which are from the collection of E. S. 
Miller. 


&: 


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TORREYA 


December, Igf4. 
Vol. 14 No, 12 


THE FLORA OF THE’ TOWN OF SOUTHOLD, LONG 
ISLAND, AND GARDINER’S ISLAND 


By Stewart H. BURNHAM AND Roy A. LATHAM 


(Continued from November TORREYA) 
PTERIDOPHYTA 


OPHIOGLOSSACEAE 
Botrychium dissectum Spreng.—Rare at Orient and East Marion. 
B. neglectum Wood—Rare at East Marion in rich woods. 
B. obliquum Muhl.—Rare. 
B. virginianum (L.) Sw. 


OSMUNDACEAE 
Osmunda cinnamomea L. 
O. Claytoniana L. 
O. regalis L. 

POLYPODIACEAE 


Adiantum pedatum L.—Rare at Orient. 

Anchistea virginica (L.) Presl—Greenport inswamps. (Woodwardia virginica (L.) 
lj 1&5 Siig) 

Asplenium platyneuron (L.) Oakes—Orient in cedar woods; also the var. serratum 
(E. S. Miller) BSP. 

Athyrium Filix-foemina (L.) Roth—Also the var. latifolium Babingt. (Asplenium 
Filix-foemina (L.) Bernh.) 

Dennstaedtia punctilobula (Mx.) Moore. 

Dryopteris Clintoniana (D. C. Eaton) Dowell—Rare. 

. cristata (L.) A. Gray—Orient. 

. hexagonoptera (Mx.) C. Chr.—Rare at Orient; also occurs at Greenport and 

Southold. (Phegopteris hexagonoptera (Mx.) Fee.) 

. intermedia (Muhl.) Gray—Orient. 

. marginalis (L.) A. Gray—Rare at Orient. 

. noveboracensis (L.) A. Gray—Orient. 

. simulata Davenp.—Orient. 

. Spinulosa (Muell.) Ktze.—Orient. 

. Thelypteris (L.) A. Gray. 

Lorinseria areolata (L.) Presl.—Greenport in swamps. (Woodwardia areolata (L.) 
Moore.) 


Se 


SAS) 1S] ISPS) 1 


{No. 11, Vol. 14 0f TorREYA, comprising pp. 201-228, was issued 27 November 1914] 


229 


230 


Onoclea sensibilis L. 

Polypodium vulgare L.—Mattituck. 

Polystichum acrostichoides (Mx.) Schott.—Orient. 
Pieridium aquilinum (L.) Kuhn. 


EQUISETACEAE 


Equisetum arvense L. 
; LYCOPODIACEAE 


Lycopodium complanatum L.—Rare at Greenport. 

L. inundatum L.—Rare at Southold, the var. Bigeloviz Tuck. 

L. lucidulum Mx.—Rare at Greenport. 

L. obscurum L.—Rare at Greenport, the var. dendrodeum (Mx.) D. C. Eaton. 


SELAGINELLACEAE 
Selaginella rupestris (L.) Spring —Rare at Orient in sandy soil, Noy., 1910 and 
IQII. 
SPERMATOPHYTA 


GYMNOSPERMAE 


PINACEAE 
Juniperus sibirica Burgsd.—Rare at Southold on sandy hills. (Juniperus nana 
Willd.) 
J. virginiana L.—Prostrate forms also occur. 
Picea rubens Sargent.—Rare at Orient. 
Pinus rigida Mill. 


ANGIOSPERMAE 
MONOCOTYLEDONES 
TYPHACEAE 
Typha angustifolia L. 
T. latifolia L. 
SPARGANIACEAE 


Sparganium americanum Nutt.—Rare at Greenport in a stream. 
S. androcladon (Engelm.) Morong—Greenport. 

S. diversifolium Graeb.—Rare at Southold, 8 Aug., 1910. 

S. eurycarpum Engelm.—Rare on Gardiner’s Island. 


ZANNICHELLIACEAE 


Potamogeton Oakesianus Robbins—Greenport and Southold in*ponds. 
P. pusillus L.—Greenport in a shallow pond. ~ 
Ruppia maritima L.—Salt-water ponds and creeks. 


ZOSTERACEAE 


Zostera marina L. 
SCHEUCHZERIACEAE 


Triglochin maritima L.—Salt marshes. 


ALISMACEAE 


Alisma subcordatum Raf.—(Formerly confused with Alisma_Plantago-aquatica L.) 
Sagittaria latifolia Willd.—Rare and variable. 


231 


GRAMINEAE 


Agropyron repens (L.) By.—Meadows and cultivated soil. 

Agrostis alba L.—Also the var. vulgaris (With.) Thurb. 

A. canina L.—Orient. 

A. hyemalis (Walt.) BSP.—Wooded swamps and brackish meadows; determined 
in part by Mrs. Agnes Chase. 

A. maritima Lam.—Salt marshes; determined in part by Mrs. Chase. 

Alopecurus pratensis L.—Rare at Orient in a low field; determined at the New 
York Botanical Garden. 

Ammophila arenaria (L.) Link—Orient. 

Andropogon furcatus Muhl.—Orient in shaded places. 

A. glomeratus (Walt.) BSP.—Rare at Orient. 

Anthoxanthum odoratum L. — 

Aristida dichotoma Mx. 

A. gracilis Ell.—Orient in meadows; specimens in N. Y. State Herbarium. 

A. purpurascens Poir—Rare at Gardiner’s Island; specimens in N. Y. State Her- 
barium. 

Arrhenatherum elatius (L.) By.—Determined in part by Mrs. Chase. 

Aspris caryophyllea (L.) Nash—Greenport. (Aira caryophyllea L.) 

Bromus hordeaceus L.—Orient in sandy soil. 

B. purgans L.—Rare at Orient. 

B. racemosus L.—Rare at Orient. 

B. secalinus L.—Cultivated grounds; determined in part by Mrs. Chase. 

B. tectorum L.—Rare at Orient in sandy soil. 

Calamagrostis canadensis (Mx.) Bv.—Low grounds. 

Cenchrus tribuloides L.—Rare at Orient and Gardiner’s Island. 

Chaetochloa glauca (L.) Scribn.—Orient in cultivated soil. 

C. imberbis (Poir.) Scribn.—Salt marshes. 

C. italica (L.) (Scribn.)—Escaped from cultivation at Orient. 

C. viridis (L.) Scribn. 

Cinna arundinacea _.—Greenpott. 

C. latifolia (Trev.) Griseb.—Greenport; specimens in N. Y. State Herbarium. 

Cynosorus cristatus L.—Rare at Orient in tvaste places. 

Dactylis glomerata L.—Meadows. 

D. anthonia spicata (L.) By.—Determined in part by Mrs. Chase. 

Deschampsia flexuosa (L.) Trin. 

Distichlis spicata (L.) Greene 

Echinochloa Crus-galli (L.) By. 

FE. Waltert (Pursh) Nash. 

Eleusine indica (L.) Gaertn. 

Elymus canadensis .—Beaches. 

E. virginicus L.—Salt marshes. 

Eragrostis Eragrostis (L.) Karst. 

E. major Host.—Rare at Orient. 

E. pectinacea (Mx.) Steud.—Orient on hillsides. 

E. pilosa (L.) By.—Rare at Orient along roads. 

Festuca capillata Lam.—Orient in meadows; determined by Mr. P. L. Ricker. 

F. elatior L. 


232 


#. nutans Willd.—Orient. 

£. octoflora Walt.—Orient in light soil. 

F. ovina L.—Orient; also the var. pseudovina Hack., on sandy beaches, determined 
by Mrs. Chase. 

Homalocenchrus oryzoides (L.) Poll.—About swamps and ponds. 
H. virginicus (Willd.) Britton—Greenport. 

Hordeum jubatum L.—Rare at Orient. 

Lolium perenne L.—Orient in a meadow. 

Muhlenbergia mexicana (L.) Trin. 

M. Schrebert Gmeln.—Orient in cedar woods. 

M. umbrosa Scribn.—Low woods. (Muhlenbergia sylvatica Torr.) 

Nothoholcus lanatus (L.) Nash—(Holcus lanatus L.) 

Panicularia acutiflora (Torr.) Ktze-——Orient about ponds. 

P. grandis (Wats.) Nash—Determined by Mrs. Chase. 

P. nervata (Willd.) Ktze—Greenport in wooded swamps; also the var. parviflora 
(Vasey) in moist woods. 

Panicularia pallida (Torr.) Ktze.—Greenport. 

P. septentrionalis (Hitchc.) Bicknell—Greenport in wet woods, specimens with 
very long panicles. 

Panicum agrostoides Spreng.—Orient; specimens in N. Y. State Herbarium. 

P. amarum Ell.—Southold on sandy beaches; specimens in N. Y. State Herbarium. 
P. Ashei Pearson—Orient; determined by Mrs. Chase. 

P. Bicknellii Nash. 

P. Boscii Poir. 

P. capillare L.—A weed in cultivated soil. 

P. cladestinum L. 

P. columbianum Scribn.—Determined by Mrs. Chase. 

P. Commonsianum Ashe—Determined by Mrs. Chase. 

P. depauperatum Muhl.—Sandy soil; determined by Mrs. Chase. 

P. dichotomiflorum Mx.—Cultivated soil. (Formerly confused with Panicum 
proliferum Lam.) 

-P. dichotomum L.—Determined by Mrs. Chase. 

P. huachucae Ashe—Sandy soil; also the var. silvicola Hitchc. & Chase, determined 
by Mrs. Chase. 

_P. implicatum Scribn. 

_P. meridionale Ashe—Determined by Mrs. Chase. (Panicum oricola Hitche. & 
Chase.) 

-~P. microcarpon Muhl.—Rare at Greenport, also “‘a rare form with pubescent 
spikelets’’ in cedar woods at Orient; determined by Mrs. Chase. (Panicum 
‘barbulatum Nash.) 

PL. polyanthes Schultes—Determined by Mrs. Chase. 

P. Scribnerianum Nash—Hilly pastures at East Marion. 

P. sphaerocarpon Ell.—Greenport; determined by Mrs. Chase. 

P.-spretum Schultes—Orient in wet meadows; reported in N. Y. State Mus. Bull. 
Orn 2 7 LOLO: 

P. verrucosum Muhl.—Rare at Orient. 

P. virgatum L.—Margins of salt marshes; determined in part by Mrs. Chase. 

Paspalum circulare Nash—Greenport and East Marion; specimens in N. Y. State 

Herbarium. 


233 


P. Muhlenbergii Nash. 

P. psammophilum Nash. 

P. setaceum Mx.—Specimens in N. Y. State Herbarium. 

Phleum pratense L. 

Phragmites Phragmites (L.) Karst.—Orient in swamps. 

Poa annua L. 

P. compressa L.—Sandy soil. 

P. pratensis L.—Meadows. 

P. triflora Gilib.— Orient about ponds; determined in part by Mrs. Chase. (Form- 
erly confused with Poa flava L.) 

Savastana odorata (L.) Scribn.—Wet meadows. 

Schizachyrium scoparium (Mx.) Nash—(Andropogon scoparius Mx.) 

Sorghastrum nutans (L.) Nash—Orient in moist woods. 

Spartina Michauxiana Hitche. 

S. patens (Ait.) Muhl.—Also var. juncea (Mx.) Hitche.; specimens in N. Y. State 
Herbarium. 

S. stricta (Ait.) Roth—The var. alterniflora (Lois.) A. Gray. 

Sphenopolis pallens (Spreng.) Scribn.—Rare at Orient. (Halonia pennsylvanica 

(DC.) Gray.) 
Sporobolus asper (Mx.) Kunth—Orient. 
S. cryptandrus (Torr.) A. Gray—Sandy beaches; reported in N. Y. State Mus. 
Bull. 150: 49. I9IT. 

Sporobolus uniflorus Muhl.—Greenport. (Sporobolus serotinus (Torr.) A. Gray.) 

S. vaginaeflorus Torr.—Orient. 

Stipa avenacea L.—Rare at East Marion and Southold; specimens in N. Y. State 
‘Herbarium. 

Syntherisma Ischaemum (Schreb.) Nash—(Syntherisma linearis (Krock.) Nash.) 

Tridens flava (L.) Hitche.—Dry soil. 

Triplasis purpurea (Walt.) Chapm.—Sandy hills. 

Tripsacum dactyloides L.—Upper edge of salt marsh at Orient, 19 July, 19009; 
specimens in N. Y. State Herbarium. 


CYPERACEAE 
Carex albolutescens Schwein. 


C. albursina Sheldon—Greenport. 

C. blanda Dew.—Orient. 

C. canescens L..—Also the var. disjuncta Fernald; specimens of the variety in N. VY. 
State Herbarium. 

. cephalophora Muhl.—Shaded places. 

. comosa Boott.—Margins of swamps. 

. complanata Torr.—(Carex triceps, var. hirsuta (Willd.) Bailey.) 

. crinita Lam.—Swampy places. 

. digitalis Willd.—Dry open woods. 

. festucacea Schkuhr.—The var. brevior (Dew.) Fernald; determined at Bureau 
of Plant Industry. 

C. flexuosa Muhl.—Greenport. (Carex tenuis Rudge.) 

C. foenea Willd. 

C. folliculata L.—Greenport in swampy woods; also a slender form. 

C. grisea Wahl.—Determined at Bureau of Plant Industry. 


QE OY OY © 


OHA Igy hol @) oI 


Q 


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C- 
‘Ee 
es 


AN VOGHOOMaprac 


234 


hormathodes Fernald—Wet places. 

intumescens Rudge—Greenport. 

lasiocarpa Ehrh.—Greenport. (Carex filiformis L.) 

Leersiit Willd.—Orient in swamps; also Carex stellulata, var. excelsior (Bailey) 
Fernald. 


. lupulina Muhl.—Wet woods; also the var. pedunculata Dew. 
. lurida Wahl.—Wet places; also the var. parvula (Paine) Bailey. 
. Muhlenbergii Schkr.—Dry open woods; in part determined at Bureau of Plant 


Industry. 


. pallescens L.—Orient in moist soil; plants with spikes on longer stalks than 


usual. 
pennsylvanica Lam.—Orient and East Marion in dry woods. 


. rosea Schkr.—Hilly woods. 


vosaeoides E. C. Howe—Orient. (Carex seorsa E. C. Howe.) 


. rostrata Stokes—Wet places. (Carex utriculata Boott.) 
. scoparia Schkr.—Low grounds. 


silacea Olney—Salt marshes. 

squarrosa L.—Greenport. 

stipata Muhl.—Greenport in wet woods. 

straminea Willd.—Orient. 

stricta Lam. 

typhina Mx.—Greenport. (Carex typhinoides Schwein.) 

varia Muhl.—Greenport. 

vestita Willd.—Orient in open woods and moist soil. 

virescens Muhl.—Dry open woods; in part determined at Bureau of Plant 
Industry. 

vulpinoidea Mx.—Sandy hillsides and low woods. 

Willdenowit Schukr.—Determined at Bureau of Plant Industry. 


. dentatus Torr.—Rare at Orient. 
. diandrus Torr.—Wet places and near the beach. 
. esculentus L.—Greenport. 


ferax L. C. Richard.—Rare near the beach; specimens in N. Y. State Her- 
barium. 


. filiculmis Vahl—Sandy hillsides and beaches. 
. filicinus Vahl—Low grounds and beaches; specimens in N. Y. State Herbarium. 


(Cyperus Nuttallii Eddy.) 

Grayi Torr.—Southold; specimens in N. Y. State Herbarium. - 
Houghtoni Torr.—Orient. 

strigosus L.—Low grounds; also the var. capitatus Boeckl. 


Dulichium arundinaceum (L.) Britton—Swamps. 
Eleocharis acicularis (L.) R. & S. 


leoicolmles ial coll eofil es) 


. acuminata (Muhl.) Nees—Greenport. 

. intermedia (Muhl.) Schultes—Greenport. 

. olivacea Torr.—Greenport in a cat-tail swamp; also Orient. 

. obtusa (Willd.) Schultes—In part determined at Bureau of Plant Industry. 
. palustris (L.) R. & S.—Greenport in wet places. 

. tenuis (Willd.) Schultes—Swampy places. 


Eriophorum virginicum L.—Rare at Orient in wet places. 


235 


Fimbristylis autumnalis (L.) R. & S.—Wet places. 

F. castanea (Mx.) Vahl—Rare at Orient on salt marshes; plants with shining(!) 
scales were collected 14 July 1913; specimens in N. Y. State Herbarium. 

Mariscus mariscoides (Muhl.) Ktze.—(Cladium mariscoides (Muhl.) Torr.) 

. Rynchospora corniculata (Lam.) A. Gray—Rare at Orient, the var. macrostachya 
(Torr.) Britton. 

R. glomeratia (L.) Vahl—Low grounds. 

Scirpus americanus Pers.—Salt marshes and beaches. 

S. atrovirens Muhl.—Orient. 

S. cyperinus (L.) Kunth—Wet places in open woods; also Scirpus pedicellatus 

Fernald. 

. Olneyt A. Gray—Southold; specimens in N. Y. State Herbarium. 

. paludosus A. Nels.—Orient on salt marshes. 

. robustus Pursh. 

. validus Vahl. 

Stenophyllus capillaris (L.) Britton—Sandy hillsides. 


AHRHN 


ARACEAE 
Acorus calamus L. 


Arisaema triphyllum (L.) Torr. 
Peliandra virginica (L.) Kunth—Greenport in wet woods. 
Spathyema foetida (L.) Raf.—Greenport. 


LEMNACEAE 


Lemna minor L.—Greenport, floating on pools. 


XYRIDACEAE 


Xyris caroliniana Walt.—Southold. 


ERIOCAULACEAE 


Eriocaulon septangulare With.—Southold. 


COMMELINACEAE 


Commelina communis L.—Roadsides and waste places. 


PONTEDERIACEAE 


Pontederia cordata L.—Greenport and Southold. 


JUNCACEAE 
Juncoides campestre (L.) Ktze. 


Juncus acuminatus Mx. 

. articulatus L.—Greenport. 

. balticus Willd.—Brackish meadow at Orient, 30 May, 1g9io, and 3 June, 1914. 
. bufonius L.—Margin of salt marshes; specimens in N. Y. State Herbarium. 

. canadensis J. Gay. 

dichotomus Ell.—Orient in cultivated field and in swamps, the var. platyphyllus 
Wieg.; in part determined at Bureau of Plant Industry. 

effusus L. 

. Gerardi Lois.—Salt marshes; used for hay. 

. Greenei Oakes & Tuck.—Orient on hills. 

. marginatus Rostk.—Rare. 


GUuUuy 


Yuu 


236 


J. pelocarpus E. Meyer—Wet places. 

J. scirpoides Lam.—Orient. 

J. secundus By.—Orient about wet places. 

J. tenuis Willd.—Also a few-flowered form; and the var. anthelatus Wieg., deter- 
mined at Bureau of Plant Industry. 


MELANTHACEAE 


Veratrum viride Ait—Greenport and Gardiner’s Island. 


LILIACEAE 


Allium canadense L.—Rare at Orient in dry woods. 

A. vineale L.—Orient. 

Hemerocallis fulua L.—Orient, escaped along roads. 
Lilium canadense L. 

L. superbum L.—Orient. 

L. tigrinum Andr.—Escaped to roadsides and meadows. 
Ornithogalum umbellatum L.—Escaped at Orient. 


CONVALLARIACEAE 
Asparagus officinalis L. 
Polygonatum biflorum (Walt.) Ell. 
P. commutatum (R. & S.) Dietr. 
Unifolium canadense (Desf.) Greene. 
Uvularia perfoliata L. 
U. sessilifolia L. 
Vagnera racemosa (L.) Morong—Some of the plants unusually pubescent (!); 
specimens in N. Y. State Herbarium. 


V. stellata (L.) Morong. 
TRILLIACEAE 
Medeola virginiana L. 


Trillium cernuum L.—Rare at Greenport. 


a 


SMILACEAE 
Smilax glauca Walt. 
S. herbacea L. 
S. rotundifolia L. 
AMARYLLIDACEAE 
Hypoxis hirsuta (L.) Coville. 
DIOSCOREACEAE 


Dioscorea villosa L.—Rare on Gardiner’s Island. and at Southold in moist woods. 


IRIDACEAE 


Iris prismatica Pursh—Orient; specimens in N. Y. State Herbarium. 

I. versicolor L. 

Sisyrinchium angustifolium Mill. 

S. atlanticum Bicknell—Orient. 

S. graminoides Bicknell—Rare at Greenport in moist woods; determined at Bureau 
of Plant Industry. 

ORCHIDACEAE © 

Blepharigloitis blephariglottis (Willd.) Rydb.—Orient in bogs; determined at the 

New York Botanical Garden. 


237 


B. lacera (Mx.) Farwell. 

Fissipes acaulis (Ait.) Small—Rare at East Marion and Southold. (Cypripedium 
acaule Ait.) 

Ibidium cernuum (L.) House—Orient. (Spiranthes cernua (L.) Richard.) 

I. gracile (Bigel.) House. 

I. praecox (Walt.) House—Specimens in N. Y. State Herbarium. 

Limodorum tuberosum L.—Rare at Orient. 

Peramium pubescens (Willd.) MacM. 

Perularia flava (L.) Farwell—Rare at Orient; determined at New York Botanical 
Garden. 

Tipularia uniflora (Muhl.) BSP.—Rare at Greenport, 21 Aug. (flowers) and 
30 Oct. (fruit), 1911; ‘‘a colony of about 30 plants’’; reported in N. Y. State 
Mus. Bull. 157: 42. 1912. The 19 July, 1914, Mr. Latham spent fully two 
hours hunting for Tipulavia before he was successful; so perfectly does the 
little dark-colored stem blend with the surrounding dead laurel twigs that one 
almost loses it when they remove the eye from it. The 24 Aug. 1914, it was 
decided that a forest fire had destroyed the colony of 30 plants; for the corms 
were exposed more than one-half out of the ground. 


DICOTYLEDONES 


JUGLANDACEAE 


Hicoria alba (L.) Britton—Rare; specimens in N. Y. State Herbarium. 
H. cordiformis (Wang.) Britton—(Hicoria minima (Marsh.) Britton.) 
H. glabra (Mill.) Britton. 
H. ovata (Mill.) Britton. 

MyRICACEAE 
Comptonia peregrina (I..) Coult.—East Marion. 
Myrica carolinensis Mill. 


SALICACEAE 


Populus alba L.—Roadsides and in woods. 

. candicans Ait.—Rarely escaped at Orient. 

. deltoides Marsh.—Roadsides and open woods. 
. heterophylla L.—Greenport in a swamp. 

. grandidentata Mx.—Moist woods. 

. italica Moench.—Rarely escaped at Orient. 

. tremuloides Mx. 

Salis alba L. 

S. Bebbiana Sarg.—Wet meadows and swamps. 
S. cordata Muhl.—Rare at Orient in swamps. 

S. discolor Muhl.—Rare at Orient. 

S. fragilis L. 

S. humilis Marsh.—Dry soil. 

S. interior Rowlee—Rare at Orient in wet places. (Salix longifolia Muhl.) 
S. lucida Muhl.—Rare at Orient. 

S. nigra Marsh.—Rare in low grounds. 

S 

S 


he} Nie) Ie) as} Hast Py) 


. purpurea L.—Escaped at Orient; specimens in N. Y. State Herbarium. 
. sericea Marsh.—East Marion. 


238 


BETULACEAE 


Alnus incana (L.) Willd.—Greenport. 
A. rugosa (DuRoi) Spreng.—Rare at Orient. 
Betula lenta L.—Greenport. 
B. populifolia Marsh. 
Corylus americana Walt.—Rare at Orient. 
C. rostrata Ait.—Orient. 
Osirya virginiana (Mill.) Willd. 
FAGACEAE 
Castanea dentata (Marsh.) Borkh. 


Fagus grandiflora Ehrh.—Greenport, East Marion and Southold; unknown at 
Orient. (Fagus americana Sweet.) 
Quercus alba L.—More common at Greenport than at Orient. 


Q. bicolor Willd.—Greenport. 
Q. coccinea Wang. 
QO. Muhlenbergit Engelm.—Rare at Greenport. 
Q. palustris DuRoi—Rare. 
Q. Prinus L.—More common at Greenport than at Ol1ient. 
Q. rubra L.—Rare. ‘ 
Q. stellata Wang.—Sandy soil. 
Q. velutina Lam. 

ULMACEAE 
Celtis occidentalis L. 

MORACEAE 


Toxylon pomiferum Raf.—Escaped from cultivation. 


CANNABINACEAE 


Humulus Lupulus L.—Rare at Orient in open woods. 


URTICACEAE 


Boehmeria cylindrica (L.) Sw. 
Pilea pumila (L.) A. Gray. 
SANTALACEAE 


Comandra umbellata (L.) Nutt.—Light sandy soil. 


ARISTOLCCHIACEAE 


Asarum canadense L.—Determined at New York Botanical Garden. 


POLYGONACEAE 


Persicaria Hydropiper (L.) Opiz—Cultivated fields and about yards. (Polygonum 
Hydropiper L.) 

P. hydropiperoides (Mx.) Small—About ponds and wet places. 

P. lapathifolia (L.) S. F. Gray—Rare at Orient. 

P. pennsylvanica (L.) Small. 

P. Persicaria (L.) Small. 

P. punctata (Ell.) Small—Fields, waste places and about swamps. 

Polygonella articulata (L.) Meisn.—Orient. 

Polygonum aviculare L.—Yards and roadsides; sometimes on sandy beaches far 
from dwellings. 


239 


P. buxiforme Small—Beaches; specimens in N. Y. State Herbarium. (Formerly 
confused with Polygonum littorale Link.) 

P. erectum ..—Orient in yards and on beaches. 

P. maritimum L.—Beaches on Gardiner’s Island; specimens in N. Y. State Her- 

barium. 

P. prolificum (Small) Robins.—Orient; specimens in N. Y. State Herbarium. 

P. tenue Mx.—Rare at Orient. 

Tiniaria Convolvulus (L.) Webb & Moqg.—Plants with the achene more shining 
than usual (!). (Polygonum Convolvulus L.) 

T. dumetorum (L.) Opiz—Rare at Orient. 

T. scandens (L.) Small. 

Tovara virginiana (L.) Raf.—Gardiner’s Island and rare at Greenport. (Poly- 
gonum virginianum L.) 

Tracaulon arifolium (L.) Raf.—Swampy woods. (Polygonum arifolium L.) 

T. sagittatum (L.) Small—Gardiner’s Island. 

Rumex Acetosella L. 

. Brittanica L.—Rare at Greenport in a swamp. 

. crispus L. 

. hastatulus Muhl. 

. obtusifolius L. 

. pallidus Bigel—Rare at Orient; reported in N. Y. State Mus. Bull. 139: 209. 

IQIO. 
. persicarioides L.—Rare at Orient. 
. verticillatus L.—Rare at Greenport. 


AAA A 


aw 


AMARANTHACEAE 


Acnida tuberculata Moq.—Rare at Greenport, margin of marshes. 
Amaranthus blitoides S. Wats.—Rare at Orient in waste places. 
A. graecizans L. 

A. hybridus L. 


A. retroflexus L. 
CHENOPODIACEAE 


Atriplex arenaria Nutt.—Orient on beaches and salt marshes. 

A. hastata L.—Beaches and salt marshes; also Atriplex littoralis L., specimens in 
N. Y. State Herbarium. 

Chenopodium album L. 

C. ambrosioides L. 

C. glaucum L.—Orient, 10 Oct. I910,a recent introduction from New York City 
in stable manure. 

C. hybridum L.—Orient on sandy beaches and salt marshes. 

C. leptophyllum (Moq.) Nutt.—Orient on sandy beaches. 

C. urbicum L.—Orient. 

Dondia maritima (L.) Druce. 

Salicornia ambigua Mx. 

S. Bigelovit Torr. 

S. europaea L.—The Salicornias determined by Dr. C. H. Peck. 

Salsola Kali L.—Specimens in N. Y. State Herbarium. 


240 


PHYTOLACCACEAE 


Phytolacca americana ..—(Phytolacca decandra L.) 


i AIZOACEAE 
Mollugo verticillata L. 


Sesuvium maritimum (Walt.) BSP.—Gardiner’s Island; specimens in N. Y. State 

Herbarium. 
PORTULACACEAE 
Claytonia virginica L.—Rare at East Marion. 
Portulaca oleracea L. 
ALSINACEAE 

Alsine graminea (L.) Britton—Rare at Orient. 

A. media L. 

Arenaria serpyllifolia L..—Orient. 

Cerastium viscosum L.—Reported in N. Y. State Mus. Bull. 139: 33. 1910. 

C. vulgatum L. ‘ 

Honkenya peploides (L.) Ehrh.—Orient on beaches; specimens in N. Y. State 
Herbarium. (Arenaria peploides L.) 

Moehringia lateriflora (L.) Fenzl. 

Sagina decumbens (Ell.) T. & G.—Rare at East Marion; reported in N. Y. State 
Mus. Bull. 150: 48. tIo1r. 

S. procumbens L. 

Spergula arvensis L. 

Tissa marina (L.) Britton—Specimens in N. Y. State Herbarium. 

T. rubra (L.) Britton—Rare at Orient. 


CARYOPHYLLACEAE 
A grostemma Githago L. 


Dianthus Armeria L. 

Lychnis alba Mill.—Roadsides. 

L. Coronaria (.) Desr.—Rare at Orient. 

L. dioica L. —Rare at Orient. 

Saponaria officinalis L. 

Silene antrirhina L. 

S. caroliniana Walt.—Orient and Southold in sandy soil. 
S. latifolia (Mill.) Britten & Rendle—Rare. 

S. noctiflora L.—Rare at Orient. 

S. stellata (..) Ait.—Rare at Orient. 

Vaccaria Vaccaria (L.) Britton—Rare at Orient..- 


NYMPHAEACEAE 
Castalia odorata (Dryand.) Woody. & Wood. 


MAGNOLIACEAE 


Liriodendron Tulipifera L.—Rare at Greenport. 


RANUNCULACEAE 
Anemone quinquefolia L. 


A. virginiana L. 
Aquilegia canadensis L.—Rare at Orient. 


241 


Caltha palustris L—Rare at Southold in wet places. 

Clematis virginiana L. 

Halerpestes Cymbalaria (Pursh) Greene—Waste places at Orient; determined at 
Bureau of Plant Industry. (Ranunculus Cymbalaria Pursh.) 

Ranunculus abortivus L.—Rare at Orient. 

R. acris L.—Rare at Greenport and Southold. 

R. bulbosus L. 

R. delphinifolius Torr.—Rare at Orient. 

R. recurvatus Poir.—Greenport; plants with a bulbous base (!). 

R. sceleratus L.—Rare at Greenport and Southold in muddy places. 

Thalictrum polygamum Muhl. 

T. revolutum DC.—Orient. (Thalictrum purpurascens Am. auth.) 


. 


BERBERIDACEAE 
Berberis vulgaris L. 


LAURACEAE 
Benzoin aestivale (L.) Nees—Greenport and Gardiner’s Island in wet woods. 
Sassafras Sassafras (L.) Karst. 


PAPAVERACEAE 
Glaucium Glaucium (L.) Karst.—Rare at Orient; but frequent on Gardiner’s Island. 
Papaver Rhoeas L.—Rare at Orient. 
P. somniferum L.—Rare at Orient. 


CRUCIFERAE 


Alyssum alyssoides L.—Rare at Orient; determined at Bureau of Plant Industry. 

Arabis glabra (L.) Bernh.—Sandy soil (purplish plants). 

Armoracia Armoracia (L.) Britton—Rare at Orient. (Roripa Armoriacia (L.) A.S. 
Hitchce.) 

Barbarea Barbarea (L.) MacM. 

B. verna (Mill.) Aschers—Rare at Orient; determined at Bureau of Plant Industry. 

Berteroa incana (L.) DC.—Rare at Orient in meadows. 

Brassica campestris ..—Cultivated fields. 

B. juncea (L.) Cosson—Rare at Orient. 

B. Napus L. 

B. nigra (L.) Koch—Rare in waste ground. 

Bursa Bursa-pastoris (L.) Britton. 

Cakile edentula (Bigel.) Hook.—Upper edge of salt marshes. 

Camelina sativa (L.) Crantz—Orient in grain fields; reported in N. Y. State Mus. 
Bull. 150: 24. Iotmt. 

Cardamine arenicola Britton—Greenport; specimens in N. Y. State Herbarium. 

C. pennsylvanica Muhl.—Orient in muddy places. 

Draba verna L.—Dry hilly shaded places. 

Erysimum officinale L.—(Sisymbrium officinale (L.) Scop.) 

Koniga maritima (L.) R. Br.—Rare at Orient. 

Lepidium campestre (L.) R. Br.—Meadows. 

L. densiflorum Schrad.—Rare at Orient. (Formerly confused with Lepidium 
apetalum Willd.) 

L. sativum L.—Meadows. e 


242 


L. virginicum L. 

Norta altissima (L.) Britton—Rare at Orient in meadows. (Sisymbrium altisst- 
mum LL.) 

Radicula palustris (L.) Moench—(Roripa palustris (L.) Bess.) 

Raphanus Raphanistrum L. 

R. sativus L.—Grain fields. 

Sinapis arvensis ..—(Brassica arvensis (L.) BSP.) 

Sisymbrium Nasturtium-aquaticum L.—Rare at Orient. (Roripa Nasturtium (L.} 

Rusby.) 
Sophia Sophia (L.) Britton—Rare at Orient. 


DROSERACEAE 
Drosera intermedia Hayne 


D. rotundifolia L.—Rare at Southold. 


CRASSULACEAE 
Sedum triphyllum (Haw.) S. F. Gray—Rare. (Sedum telephium Am. auth.) 


SAXIFRAGACEAE 


Micranthes virginiensis (Mx.) Small—Rare at Orient. (Saxifraga virginiensis Mx.) 


HAMAMELIDACEAE 


Hamamelis nivirgiana L.—Greenport, Southold and Gardiner’s Island in moist 
woods; no Orient records. 


GROSSULARIACEAE 


Grossularia Cynosbati (L.) Mill.—Orient in woods. (Ribes Cynosbati L.) 
G. oxyacanthoides (L.) Mill. 
Ribes vulgare Lam.—Orient. (Formerly confused with Ribes rubrum L.) 


PLATANACEAE 


Platanus occidentalis L. 
ROSACEAE 


Agrimonia gryposepala Wallr. 

Argentina Anserina (L.) Rydb.—Orient and Gardiner’s Island on beaches and 
salt marshes. 

Fragaria vesca L.—Woods. 

F. virginiana Duchesne—Hills and swamps (variable). 

Geum canadense Jacq. 

Geum flavum (Porter) Bicknell—Greenport. 

G. virginianum L. 

Potentilla argentea L.—Orient. 

P. canadensis L. 

P. monspeliensis L. 

P. pumila Poir.—Orient and East Marion. 

P. simplex Mx.—Orient. 

Rosa carolina L.—Sometimes the bushes are almost wholly unarmed. 

R. cinnamomea L.—Rarely escaped at Orient. 

R. rubiginosa L.—Sandy soil and shaded places. 

R. rugosa Thunb.—Rarely escaped at Orient on sandy beaches; determined at 
Bureau of Plant Industry. 


243 


R. virginiana Mill.—Both forms occur, Rosa humilis Marsh. and Rosa lucida Ehth. 
Rubus alleghaniensis Porter. 
R. hispidus L.—Sandy bogs. 
R. occidentalis L. 
R. phoenicolasius Maxim.—Orient, established in woods. 
R. procumbens Muhl. 
R. strigosus Mx. 
Sanguisorba canadensis L.—Greenport in wet woods. 
Spirea latifolia (Ait.) Borkh.—Wet places. 
S. tomentosa L.—Orient. 
MALACEAE 
Amelanchier canadensis (L.) Medic. 
Aronia arbutifolia (L.) Ell.—Orient. 
A. atropurpurea Britton. 
A. melanocarpa (Mx.) Britton.—Orient. 
Crataegus chrysocarpa Ashe—Rare at Orient. (Crataegus rotundifolia (Ehrh.) 
Borkh.) 
C. Crus-Galli L. 
C. monogyna Jacq.—Rare at Greenport. (Formerly confused with Crataegus 
Oxyacantha L.) 
Malus Malus (L.) Britton. 
AMYGDALACEAE 
Padus virginiana (L.) Mill.—(Prunus serotina Ehrh.) 
Prunus americana Marsh.—Rare at Orient. 
P. Avium L.—Roadsides. : 
P. Cerasus L.—Wood margins. 
P. domestica L.—Rare, a degenerate form. 
P. maritima Wang.—Rare at Greenport; but more abundant at Orient, Southold 
and Gardiner’s Island. 
CAESALPINIACEAE 
Chamaecrista fasciculata (Mx.) Greene. 
Gleditschia triacanthos L.—Rare at Orient. 


FABACEAE 
Baptisia tinctoria (L.) R. Br. 
Coronilla varia L.—Rare at Greenport; specimens in N. Y. State Herbarium. 
Cracca virginiana L.—Mattituck. 
Falcata comosa (L.) Ktze.—Rare at Orient in rich woods. 
Glycine Apios L.—Swamps; plants sometimes with 3 leaflets. (Apios Apios (L.) - 
MacM.) 
Lathyrus maritimus (L.) Bigel. 
Lespedeza capitata Mx. 
L. frutescens (L.) Britton—Southold. 
L. hirta (L.) Hornem. 
L. procumbens Mx.—East Marion. 
L. Stuvet Nutt.—Southold. 
L. violacea (L.) Pers.—Greenport and Southold. 
L. virginica (L.) Britton—Southold. 
Lupinus perennis L.—Southold in sandy soil. 


244 


Medicago hispida Gaertn.—Rare at Greenport. 

M. lupulina L.—Greenport. 

M. sativa L.—Rare in meadows. 

Meibomia canadensis (L.) Ktze.—Rich woods. 

M. Dillenii (Darl.) Ktze.—Greenport and Southold in rich woods. 

M. grandiflora (Walt.) Ktze. 

M. nudiflora (L.) Ktze.—Southold. 

M. viridiflora (L.) Ktze—Rare at Greenport; determined at Bureau of Plant 
Industry. 

Melilotus alba Desy.—Greenpott. 

Phaseolus polystachyus (L.) BSP.—Orient in woods. 

Robinia Pseudo-Acacia L. 

R. viscosa Vent. 

Strophostyles helvola (L.) Britton—Near beaches; specimens in N. Y. State Her- 
barium. 

Trifolium agrarium L. 

T. arvense L. 

T. hybridum L.—Meadows. 

T. incarnatum L.—Rare. 

T. pratense L. 

T. procumbens L.—Rare. 

T. repens L. 

Vicia angustifolia L.—Orient; also the var. segetalis (Thuill.) Koch; reported in 
N. Y. State Mus. Bull. 150: 49. Ig1t. 

V. hirsuta (L.) Koch—Rare at Orient; determined at Bureau of Plant Industry. 


GERANIACEAE 
Erodium cicutarium (L.) L’Her.—Mattituck. 
Geranium maculatum L. 
Robertiella Robertiana (L.) Hanks—(Geranium Robertianum L.) 


OXALIDACEAE 
Xanthoxalis Britioniae Small 


X. stricta (L.) Small. 
LINACEAE 


Cathartolinum striatum (Walt.) Small—Brackish meadows and wet woods. (Linum 
striatum Walt.) 

_ C. virginianum (L.) Reichenb. 

Linum usitatissimum L.—Rare in grain fields.. 


BALSAMINACEAE 


Impatiens biflora Walt.—Greenport, Southold and Gardiner’s Island in wet places. 


SIMAROUBACEAE 
Ailanthus glandulosa Desf.—Rare at Greenport. 


POLYGALACEAE 
Polygala cruciata L.—Orient. 


P. lutea L.—Rare at Greenport. 


245 


P. paucifolia Willd.—Orient, the station destroyed by cultivation; determined at 
New York Botanical Garden. 
P. polygama Walt.—Dry open woods. 
P. verticillata L.—Dry hilly soil. 
P. viridescens L.—Moist woods. 
EUPHORBIACEAE 
Acalypha gracilens A. Gray. 
A. virginica L. 
Chamaesyce maculata (L.) Small—Cultivated fields. (Euphorbia maculata L.) 
C. polygonifolia (L.) Small. 
Tithymalus Cyparissias (L.) Hill—Roadsides. (Euphorbia Cyparissias L.) 
T. Lathyrus (L.) Hill—Rare at Orient in waste places; determined at Bureau of 
Plant Industry. 
CALLITRICHACEAE 
Callitriche heterophylla Pursh—Edge of a pond in woods at Greenport; determined 
at Bureau of Plant Industry. 
C. palustris L.—Rare at Orient in a pond, 1908; determined at New York Botanical 
Garden. Not found since and perhaps the many years of drought have killed 


the roots. 
ANACARDIACEAE 


Rhus copallina L. 
R. glabra L. 
Toxicodendron radicans (L.). Ktze.—Plants may be either low or high climbing; 
the leaves sometimes toothed. (Rhus radicans L.) 

T. vernix (L.) Ktze.—Rare. 

ILICACEAE 
Ilex bronxensis Britton—Rare at Orient; specimens in N. Y. State Herbarium. 
I. glabra (L.) A. Gray—Rare at East Marion. 
I. verticillata (L.) A. Gray. 

CELASTRACEAE 

Celastrus scandens L. 

ACERACEAE 
Acer carolinianum Walt.—Rare on Gardiner’s Island. (Acer rubrum tridens Wood.) 
A. Negundo L.—Escaped at Orient. 
A. rubrum L. 
A. saccharinum L. 

RHAMNACEAE 

Ceanothus americanus L.—Rare at Southold. 
Rhamnus cathartica L.—Orient. 

VITACEAE 
Parthenocissus quinquefolia (L.) Planch. 
Vitis aestivalis Mx. 
V. bicolor LeConte. 
V. Labrusca L.—Moist thickets. 


TILIACEAE 
Tilia americana L. 
MALVACEAE 
Abutilon Abutilon (L.) Rusby—Orient in cultivated fields. 
Hibiscus Moscheutos L. 


246 


H. Trionum L.—Rare at Greenport. 
Malva rotundifolia L. 
HYPERICACEAE 
Hypericum canadense L.—Wet meadows; specimens in N. Y. State Herbarium. 
H. majus (A. Gray) Britton—Moist places. 
A. mutilum L.—Moist places. 
H. perforatum L. 
H. punctatum Lam.—(Hypericum maculatum Walt.) 
Sarothra gentianoides L. 
Triadenum virginicum (L.) Raf. 
. CISTACEAE 
Crocanthemum canadense (L.) Britton—East Marion. (Helianthemum canadense 
(L.) Mx.) 
C. majus (L.) Britton—East Marion. 
Hudsonia tomentosa Nutt.—Orient, Southold and Gardiner’s Island on sandy 
beaches. 
Lechea intermedia Leggett—Orient. 
L. Leggettii Britt. & Holl.—Orient. 
L. maritima Leggett. 
L. racemulosa Lam.—Orient and Greenport; specimens in N. Y. State Herbarium. 


L. villosa Ell.— Dry woods. 
VIOLACEAE 
Viola cucullata Ait—Swamps. 


V. fimbriatula J. E. Sm. 
V. lanceolata L. 
V. pallens (Banks) Brainerd. 
V. papilionacea Pursh—The var. domestica Bicknell in old lawns. 
V. pedata L.—East Marion and Greenport. 
V. primulifolia L.—Greenpott. 
CACTACEAE 


Opuntia Opuntia (L.) Coult.—Rare at Orient in sandy soil. 


LYTHRACEAE 
Decodon verticillatus (L.) Ell. 
MELASTOMACEAE « 


Rhexia virginica L.—Rare at Orient. 


ONAGRACEAE 


Chamaenerion angustifolium (L.) Scop.—Rare at Orient. 
Circaea lutetiana L. 

Epilobium adenocaulon Haussk. 

FE. coloratum Muhl.—Orient. 

EF. lineare Muhl.—Rare at Orient. 

E. palustre L.—Rare at Orient. 

FE. strictum Muhl.—Rare at Orient. 

Isnardia palustris L.—Wet places. 

Kneifia Allent (Britton) Small—Orient. 

K. fruticosa (L.) Raimann—Also the var. pilosella Britton. 
K. linearis (Mx.) Spach—Orient. 

K. longipedicellata Small—Orient. 


247 


K. pumila (L.) Spach. 

Ludwigia alternifolia L—Swampy places. 
Oenothera biennis L. 

O. Oakesiana Robbins—Orient. 


HALORAGIDACEAE 


Myriophyllum humile (Raf.) Morong—Rare at East Marion. 
M. pinnatum (Walt.) BSP.—Greenport in a pond; determined by P. L. Ricker. 
Proserpinaca palustris L.—Orient. 


ARALIACEAE 
Aralia nudicaulis L. 


A. racemosa L.—Rare at Greenport. 


AMMIACEAE ~ 


Angelica atropurpurea L.—Rare at East Marion; specimens in N. Y. State Her- 
barium. . 

Cicuta maculata L. 

Daucus Carota L. 

Foeniculum Foeniculum (L.) Karst.—Escaped at Orient. 

Heracleum lanatum Mx. 

Ligusticum scoticum L.—Orient, edge of woods bordering salt marshes; reported in 
N. Y. State Mus. Bull. 139: 25. tg910. 

Pastinaca sativa L.—Rare. 

Ptilimnium capillaceum (Mx.) Raf. 

Sanicula canadensis L. 

S. marylandica L. 

Sium cicutaefolium Schrank—Swampy woods. 

Washingtonia Claytoni (Mx.) Britton—Orient; specimens in N. Y. State Herbarium. 

W. longistylis (Torr.) Britton—Rare. 


CORNACEAE 


Cornus femina Mill.—Rare at Orient but more abundant at East Marion and 
Southold. (Cornus candidissima Marsh.) 

C. stolonifera Mx.—Rare at Orient, edge of a swamp. 

Cynoxylon floridum (L.) Raf.—(Cornus florida L.) 


Nyssa sylvatica Marsh. : 
CLETHRACEAE 
Clethra alnifolia L. 

PYROLACEAE 
Chimaphila maculata (L.) Pursh. 


C. umbellata (L.) Nutt.—Rare at Orient but more common at East Marion. 
Pyrola americana Sweet. 
P. elliptica Nutt. 

MONOTROPACEAE 
Hypopitys lanuginosa (Mx.) Nutt.——In oak woods; the plants crimson. 
Monoiropa uniflora L. 

ERICACEAE 

Azalea nudiflora L.—Rare at Greenport in swamps. 
A. viscosa L.—Greenport and Orient in sandy swamps. 


248 


Epigaea repens L.—East Marion. 

Eubotrys racemosa (L.) Nutt.—Rare at Greenport inswamps. (Leucothoé racemosa 
(L.) A. Gray.) 

Gaulthera procumbens L.—Rare at Southold. 

Kalmia angustifolia L.—Mattituck. 

K. latifolia L.—East Marion and Southold. 

Uva-Ursi Uva-Ursi (L.) Britton—Orient. (Arctostaphylos Uva-Ursi (L.) Spreng.) 

Xolisma ligustrina (L.) Britton. 


V ACCINIACEAE 


Gaylussacia baccata (Wang.) K. Koch—In woods. 

Oxycoccus macrocarpus (Ait.) Pursh—Plants bearing two forms of fruit occur; 
taller plants bear oblong fruit and are rarer. 

Vaccinium angustifolium Ait.—(Vaccinium pennsylvanicum Lam.) 

V. atrococcum (A. Gray) Heller—In swamps. 

V. corymbosum L. 


V. vacillans Kalm—In woods. 
PRIMULACEAE 
Anagallis arvensis L. 


Lysimachia Nummularia L.—Rare at Orient. 
L. quadrifolia L. 
L. terrestris (L.) BSP. 
Samolus floribundus HBK.—Orient. 
Steironema ciliatum (L.) Raf—Gardiner’s Island in low woods; determined by 
Norman Taylor. 
Trientalis americana Pursh. 
PLUMBAGINACEAE 


Limonium carolinianum (Walt.) Britton. 


OLEACEAE 
Fraxinus americana L.—Greenport. 
Ligusirum vulgare L. 
Syringa vulgaris L. 
GENTIANACEAE 


Bartonia virginica (L.) BSP.—Rare. 
Sabbatia stellaris Pursh—Orient on salt marshes; specimens in N. Y. State Her- 


barium. 
APOCYNACEAE 
A pocynum androsaemifolium L. 


A. cannabinum L.—Rare at Orient; plants with the leaves lightly pubescent 
beneath. 

A. medium Greene—Rare at Orient. 

A. pubescens R. Br.—Rare at Orient; specimens in N. Y. State Herbarium. 

A. sibiricum Jacq.—(A pocynum album Greene.) 

Vinca minor L.—Roadsides at Greenport. 


ASCLEPIADACEAE 


Asclepias amplexicaulis J. E. Smith—Rare at Orient. 
A. purpurascens L.—Orient. 


249 


A. pulchra Ehrh.—Orient in low ground. 

A. syriaca 1..—Specimens in N. Y. State Herbarium. 

A. tuberosa L.—Rare at East Marion, Greenport and Southold. 
A. verticillata L.—Rare at Orient. 


CONVOLVULACEAE 
Convolvulus repens L.—Orient. 
C. sepium L.—Orient; the flowers white or pinkish. 
Ipomoea purpurea (L.) Lam.—Escaped. 


CUSCUTACEAE 


Cuscuta arvensis Beyrich—Orient and Southold. 
C. compacta Juss.—Greenport on Clethra and Cephalanthus. 
C. Gronovit Willd. 
POLEMONIACEAE 
Phlox paniculata L.—Rarely escaped at Orient. 
P. subulata L.—The two stations at Orient have recently been destroyed by culti- 
vation. 
BORAGINACEAE 
Cynoglossum officinale L.—Rare at Orient. 
Myosotis arvensis (L.) Hill—Rare at Orient in cultivated grounds; determined at 
Bureau of Plant Industry. 
M. virginica (L.) BSP.—Rare at Orient; specimens in N. Y. State Herbarium. 
Onosmodium virginianum (L.) DC.—Rare at Orient on sandy beaches. 


VERBENACEAE 
Verbena hastata L. 


V. urticifolia L.—Shaded places. 
LABIATAE 
A gastache nepetoides (L.) Ktze.—Gardiner’s Island in rich woods. 
Clinopodium vulgare L.—Gardiner’s Island in rocky woods. 
Collinsonia canadensis L.—Gardiner’s Island in rich woods. 
Glecoma hederacea L.—Rare at Orient. 
Hedeoma pulegioides (L.) Pers.—Rare in shaded places. 
Koellia flexuosa (Walt.) MacM.—Orient. 
K. mutica (Mx.) Britton—Rare at Orient. 
K. virginiana (L.) MacM.—Rare at Orient. 
Lamium amplexicaule L.—Orient in cultivated fields. 
Leonurus Cardiaca L.—Rare. 
Lycopus americanus Muhl. 
L. membranaceus Bicknell. 
L. sessilifolius A. Gray—Southold. 
L. uniflorus Mx. 
L. virginicus L. 
Marrubium vulgare L.—Orient. 
Melissa officinalis L.—Rare at Greenport. 
Mentha gentilis L.—Rare at Orient along roads. 
M. piperita L.—Rare at Orient. 
M. spicata L. 
Nepeta Cataria L. 


250 


Prunella vulgaris L. 

Scutellaria galericulata L.—Swamps. 

S. lateriflora L.—Orient and Greenport in low woods. 

‘Teucrium canadense .—Sandy beaches and rocky woods; specimens in N. Y. State 
Herbarium. 

Trichostema dichotomum L.—Plants with pink flowers (!); reported in N. Y. State 
Mus. Bull. 157: 43. I912. 

SOLANACEAE 

Datura Stramonium L.—Gardiner’s Island and elsewhere. 

Lycium halimifolium Mill.—Rare. 

Lycopersicon Lycopersicon (L.) Karst.—Escaped. ‘ 

Physalis peruviana L.—Escaped at Orient in waste places and in gardens. 

Physalodes physalodes (L.) Britton—Escaped at Orient. 

Solanum Dulcamara L.—Rare. 

S. nigrum L.—Rare on sandy beaches. 


SCROPHULARIACEAE 


Agalinis maritima Raf.—Orient on salt marshes; specimens in N. Y. State Her- 
barium. (Gerardia maritima Raf.) 
A. purpurea (L.) Britton—Orient; specimens in N. Y. State Herbarium. 
A. tenutfolia (Vahl) Raf.—Dry hills. 
‘Chelone glabra L.—Rare at Greenport. 
Dasystoma flava (L.) Wood—Greenport. 
D. pedicularia (L.) Benth.—East Marion. 
D. virginica (L.) Britton. 
Gratiola aurea Muhl.—Rare at Orient. 
Ilysanthes attenuata (Muhl.) Small—Orient. 
I. dubia (L.) Barnh.—Orient. 
Linaria canadensis (L.) Dum. 
L. Linaria (L.) Karst. 
Melampyrum lineare Lam.—The leaves are variable in outline. 
Mimulus ringens L.—Greenport. 
-~Pedicularis canadensis L.—Orient. 
-Scrophularia leporella Bicknell—Rare at Orient. 
Verbascum Blattaria L. 
WV. Thapsus L. 
‘Veronica arvensis L.—Orient. 
W. officinalis L.—East Marion. 
V. peregrina L.—Orient. 
V. serpyllifolia L. 
LENTIBULARIACEAE 
Setiscapella cleistogama (A. Gray) Barnhart—Southold; determined at Bureau of 
Plant Industry. (Utricularia cleistogama (A. Gray) Britton.) 
Stomoisia cornuta (Mx.) Raf.—Southold. (Utricularia cornuta Mx.) 


OROBANCHACEAE 


Leptamnium virginianum (L.) Raf.—Greenport. 
Thalesia uniflora (L.) Britton—Rare at Orient. 


251 


BIGNONIACEAE 


Bignonia radicans L.—Rarely escaped at Orient. (Tecoma radicans (L.) DC.) 


PHRYMACEAE 


Phryma Leptostachya L.—Gardiner’s Island and Greenport in woods. 


PLANTAGINACEAE 
Plantago aristata Mx. 


P. halophila Bicknell—Orient on salt marshes; plants earlier to flower and more 
downy than Plantage major L. 


P. lanceolata L. 

P. major L. 

P. maritima L.—Orient; specimens in N. Y. State Herbarium. 

P. media L. 

P. pusilla Pursh—Rare on dry hilltops; specimens in N. Y. State Herbarium. 
P. Rugelit Dcene.—East Marion, shores of a pond. 

P. virginica L.—East Marion in sandy soil. 


RUBIACEAE 
Cephalanthus occidentalis L. 


Galium A parine L.—Orient in low rich shaded places. 

. ciycaezans Mx.—Rich woods. 

. Claytont Mx.—Low grounds. 

. lanceolatum Torr.—Rare at Orient; determined at N. Y. Botanical Garden. 
. palustre L.—Greenport. 

. pilosum Ait.—Rare at Orient; the flowers purple. 

. tinctorium L.—Greenport in swampy woods. 

. triflorum Mx.—Greenport. 

Mitchella repens L.—Plants sometimes having unusually large leaves. 


QAAAAANA 


CAPRIFOLIACEAE 


Diervilla Diervilla (L.) MacM. 

Lonicera japonica Thunb.—Orient and East Marion in woods. 

L. sempervirens L.—East Marion. 

Sambucus canadensis L. 

sS. racemosa L.—Rare at Orient, the station now destroyed; determined at Bureau 
of Plant Industry. 

Triosteum aurantiacum Bicknell. 

T. perfoliatum L.—Rare at Orient. 

Viburnum acerifolium L.—More abundant at Greenport than at Orient. 

V. dentatum L.—‘ ‘A form with leaves decidedly acuminate’’; reported in N. Y. 
State Mus. Bull. 150: 49. Ig11. 

Y. Lentago L.—Rare at Orient. 

V. venosum Britton—Rare at East Marion in swamps; reported in N. Y. State 
Mus. Bull. 150: 41. I9II. 


VALERIANACEAE 
Valeriana officinalis L._—Orient. 


252 


CAMPANULACEAE 


Campanula rapunculoides L.—Rarely escaped at Orient. 
Specularia perfoliata (L.) A. DC.—Rare in hilly woods. 


LOBELIACEAE 


Lobelia cardinalis L.—Rare from Greenport to Southold. 
L. inflata L. 
L. syphilitica L.—Rare at Orient in low ground. 


CICHORIACEAE 


Apargia nudicaulis (L.) Britton—Specimens in N. Y. State Herbarium. (Leon- 
todon nudicaule (L.) Banks.) 

Cichorium Intybus .—Orient. 

Crepis capillaris (L.) Wallr.—Orient. (Crepis virens L.) 

C. setosa Hall. f£.—Reported in N. Y. State Mus. Bull. 150: 29. 1911. 

C. tectorum L.—Rare at Orient; determined by Dr. C. H. Peck. 

Hieracium aurantiacum L.—Rare at Orient. 

H. Gronovii L.—Orient; specimens in N. Y. State Herbarium. 

H. paniculatum L.—Greenport. 

H. scabrum Mx.—Plants with more naked stems than usual; specimens in N. Y. 
State Herbarium. 

H. venosum L. 

Hypochaeris radicata L.—Orient; specimens in N. Y. State Herbarium. 

Krigia virginica (L.) Willd.—Orient in light soil. 

Lactuca canadensis L._—Cedar woods and elsewhere; also the var. montana Britton. 

L. sagittifolia Ell.—Orient. 

L. spicata (Lam.) Hitche. 

Lapsana communis L.—Rare at Orient; determined by P. L. Ricker. 

Leontodon erythrospermum (Andrz.) Britton—Light soil and on sandy beaches at 
Orient. (Taraxicum erythrospermum Andtz.) 

L. Taraxicum L. 

Nabalus serpentarius (Pursh) Hook.—Greenport. 

N. trifoliolatus Cass. 

Picris echioides L.—Reported in N. Y. State Mus. Bull. 139: 28. Igio. 

P. hieracioides L.—Rare at Orient; determined by Dr. C. H. Peck; reported in 
N. Y. State Mus. Bull. 150: 37. I9II. 

Sonchus arvensis L.—Rare at Orient. 

S. asper (L.) Hill.—Orient. 

S. oleraceus L. 

AMBROSIACEAE 

Ambrosia elatior L.—(Ambrosia artemisiaefolia L.) 

A. trifida L.—Rare at Orient in cultivated fields. 

Xanthium commune Britton—Orient on beaches. 

X. spinosum L.—Rare on Gardiner’s Island. 


COMPOSITAE 


Achillea Millefolium L.—Also the forma rosea. 
Anaphallis margaritacea (L.) Benth. & Hook.—Rare. 


253 


Antennaria neglecta Greene. 

A. plantaginifolia (L.) Richards. 

Anthemis arvensis L.—Rare at Orient in meadows and waste places. 
A. Cotula L. 

A. tinctoria L.—Rare at Orient in meadows; specimens in N. Y. State Herbarium. 
Arctium minus Schkr. 

Ariemisia caudata Mx.—Determined by Dr. C. H. Peck. 

A. Stellariana Bess.—Orient on beaches. 

Aster cordifolius L.—Greenport. 

. divaricatus L.—Woods. 

. dumosus L.—Orient in sandy soil. 

. ericoides L.—Southold. 

. laevis L.—Low woods; also the long-leaved form. 

. lateriflorus (L.) Britton—Orient in woods. 

. macrophyllus L._—The plants are variable. 

. multifiorus Ait. 

. novae-angliae L.—More common on Gardiner’s Island than at Orient. 
novi-belgit L._—Low grounds. 

paniculatus Lam. 

patens Ait.—Dry hills. 

. puniceus L. 

. salicifolius Lam.—Orient in low places. 

. spectabilis Ait—Orient; also a form with white flowers. 

. subulatus Mx. 

. tenutfolius L. 

. Tradescanti L. 

. undulatus L. 


a el a 


. vimineus Lam. 

Baccharis halimifolia L.—Orient about salt marshes. 

Bidens cernua L. 

B. comosa (A. Gray) Wiegand—Low grounds. d 

B. conhata Muhl.—Low grounds; also a form with entire leaves. 

B. discoidea (T. & G.) Britton. 

B. frondosa L. 

B. laevis (L.) BSP. 

Centaurea Cyanus L.—Rare at Orient. 

C. Jacea L.—Rare at Orient in a dry pasture. 

Chrysanthemum Leucanthemum L. 

Chrysopsis falcata (Pursh) Ell.—Orient and Southold. 

C. mariana (L.) Ell. 

Cirsium arvense (L.) Scop. 

C. discoloy (Muhl.) Spreng. 

C. horridulum Mx.—Specimens in N. Y. State Herbarium. (Cirsium spinosissie 
mum (Walt.) Scop.) 

C. lanceolatum (L.) Hill—Moist places. 

C. muticum Mx.—Rare at Orient. 

C. odoratum (Muhl.) Britton. 

Doellingeria umbellata (Mill.) Nees. 


254 


Erechtites hieracifolia (L.) Raf.—Two forms occur, hairy and smooth plants; 
specimens in N. Y. State Herbarium. 

Erigeron annuus (L.) Pers. 

E. philadelphicus L. 

FE. pulchellus Mx. 

E. ramosus (Walt.) BSP. 

Eupatorium aromaticum L.—Southold. 

E. hyssopifolium L.—Southold. 

E. maculatum L.—Crient in low grounds. 

E. perfoliatum L. 

E. purpureum L. 

EF. verbenaefolium Mx. 

Euthamia graminifolia (L.) Nutt. 

E. tenuifolia (Pursh) Greene—Southold. 

Galinsoga parviflora Cavy.—Orient along roads; the var. hispida DC. 

Gnaphalium obtusifolium L. 

G. uliginosum L. 

Helianthus annuus L.—Rarely escaped at Orient. 

H. divaricatus L. 

H. giganteus L. 

Ai. strumosus L. 

Ai. tuberosus L. 

Lacinaria spicata (L.) Ktze.—Orient, a colony of 50 or more plants; specimens in 
N. Y. State Herbarium. 

Leptilon canadense (L.) Britton. : 

Mariana mariana (L.) Hill—Orient in a garden; specimens in N. Y. State Her- 
barium. 

Onopordum Acanthium L.—More common on Gardiner’s Island than at Orient and 
East Marion; specimens in N. Y. State Herbarium. 

Pulchea camphorata (L.) DC. 

Rudbeckia hirta L.. 

Senecio aureus L.—Rare at Orient. 

S. vulgaris L.—Rare in cultivated fields. 

Seriocarpus asteroides (L.) BSP. 

Solidago altissima L. 

. aspera Ait.—Reported in N. Y. State Mus. Bull. 139: 30. Ig10. 

. bicolor L. 

. caesia L. 

. juncea Ait.—Plants variable. 

. nemoralis Ait. 

. odora Ait. 

. rugosa Mill.—The broad-leaved form and the form with small leaves. 

. sempervirens L. 

. serotina Ait.—Orient in swamps. 

. ulmifolia Muhl. 

Tanacetum vulgare L. 

Vernonia noveboracensis (L.) Willd.—Orient. 


ARARHARHARHUAUHYA 


255 


NEWS ITEMS 


Among the botanical societies that will hold meetings in 
Philadelphia during the Christmas holidays are: Botanical Society 
of America, Society of American Bacteriologists, American Phy- 
topathological Society, American Fern Society and the Sullivant 
Moss Society. 


On Monday evening, December 14, at the meeting of the New 
York Academy of Sciences, a symposium on Porto Rico was held 
at which reports on the Academy’s exploration of that island 
were heard. Dr. N. L. Britton, Dr. Marshall A. Howe, and Dr. 
N. Wille spoke on the botanical features. The latter left for 
Porto Rico on December 19 to study the fresh-water algae. 


We learn from Science that Professor J. C. Bose, of Calcutta, 
known for his work in plant physiology, is in this country. He 
is to be in the east until January 11, on which date he addresses 
the New York Academy of Sciences, and before which time he 
will speak at various universities and to scientific bodies. Dur- 
ing the latter part of January he is arranging a trip to several 
middle western universities. On Monday, December 7, Dr. 
Bose spoke at Columbia University on ‘“‘ Physiological Response 
in Mimosa.” 


Dr. Hally D. M. Jolivette, formerly instructor of botany 
in the State College, Pullman, Washington, has recently been 
appointed a scientific assistant in the office of pathological col- 
lections and inspection work, department of agriculture. 


A Joint Committee on Standards for Graphic Presentation has 
been formed by the appointment of members from a number 
of learned societies. Botanists who have suggestions to offer 
should communicate with Dr. J. Arthur Harris, Station for 
Experimental Evolution, Cold Spring Harbor, Long Island, N.Y. 


The flora of Southhold and Gardiner’s Island which has occu- 
pied most of the November and December issues of TORREYA 
has been reprinted in pamphlet form. Copies may be procured 
from Mr. S. H. Burnham, R. F. D. No. 2, Hudson Falls, N. Y., 
at twenty-five cents each. 


INDEX* 


Aase, H., 199 

Abies, 61; concolor, 63, 64; lasiocarpa, 
61, 63; magnifica, 63 

Acarospora, 87; chlorophana, 86; dis- 
creta, 86; fuscata, 85; squamulosa, 86 

Acarosporaceae, 87 

Acer circinatum, 61; monumentale, I41; 
Negundo, 40, 42; pennsylvanicum, 61; 
rubrum, 175, 178; saccharum, 57, 140, 
183 

Aceraceae, 245 

Acetabularia caraibica, 7; crenulata, 7 

Acidodontium megalocarpum, 26 

Acolium, 78 

Actaea rubra, 183 

Actinococcus subcutaneus, 100, 101 

Adams, J., 72 

Addison Brown, I. 

Additions to the Pleistocene Flora of the 
Southern States, 159 

Adiantium pedatum, 179 

Agardhiella tenera, 98 

Agaricaceae, 216 

Ahnfeltia plicata, 99 

Aizoaceae, 240 

Alabama, The Aquatic Vegetation of 
Squaw Shoals, Tuscaloosa County, 
149 

Alectoria, 140; bicolor, 80; chalybei- 
formis, 80; Fremontii, 140; jubata, 79; 
jubata bicolor, 80; jubata chalybei- 
formis, 80; jubata implexa, 79; 
ochroleuca, 80 

Algal stalactites in Bermuda, 195 

Alismaceae, 230 

Allen,.C. F., 38 

Alnus, oregana, 61; rugosa, I5I, 153 

Alsinaceae, 240 

Amaranthaceae, 239 

Amaryllidaceae, 236 

Ambrosia, 12-15; artemisifolia, 192 

Ambrosiaceae, 252 

American Botanical Exchange Bureau, 
Sir 

American Breeder’s Magazine, The, 10 

American Genetic Association, II 

American Museum of Natural History, 
Meetings held at, 16, 49, 69, 120, 
I30, 163, 164 


American Phytopathological Society, 
38 
Ames, O., 18 


Ammiaceae, 247 

Amyegdalaceae, 243 

Anacardiaceae, 245 

Anaptychia comosa, 82 

Anderson, F., 199 

Andropogon scoparius, 171, 172, 186— 
188 

Androsace Chamaejasme arctica, 66 

Angiospermae, 230 

Antennaria plantaginifolia, 173 

Anzia colpodes, 84 

Apocynaceae, 248 

Aquatic Vegetation of Squaw Shoals, 
Tuscaloosa County, Alabama, The, 
149 

Aquilegia canadensis, 171 

Araceae, 235 

Araliaceae, 247 

Arisaema triphyllum, 179 

Aristida, 58; dichotoma, 171 

Aristolochiaceae, 238 

Artemisia candata, 189; tridentata, 60 

Arthonia astroidea, 92; glaucescens, 92; 
glebosa, 92; lecidella, 92; punctifor— 
mis, 92; radiata, 92; spectabilis, 92 

Arthoniaceae, 92 

Arthothelium spectabile, 92 

Arthrostylidium sarmentosum, 19 

Arthur, J. C., 38 

Arundinaria macrosperma, I61 

Arzberger, E. G., 12, 17 

Asarum canadense, 183 

Asclepiadaceae, 248 

Asclepias syriaca, 186, 188; verticillata, 
189 

Ascomycetes, 207 

Ascophyllum, 99 

Aspidium marginale, 177; novebora- 
cense, 179; spinulosum, 179 

Astragalus, 65; alpinus, 65 

Aster acuminatus, 45; divaricatus, 177, 
179; linariifolius, 173, 189; patens, 173 

Atriplex, 60 


Bacidia atrasanguineo, 90; chlorantha,. 
89; chlorasticta, 89; fuscorubella, 90, 


* New names and final members of new combinations in bold face type. Im 
the Flora of Southold and Gardiner’s Island, occupying most of the November 
and December issues, only family names are indexed.—ED. 


256 


257 


91; inundata, 90; rubella, 90; mus- 
corum, 89; Schweinitzii, 90; umbrina, 
90 

Baeomyces aeruginosus, 81, 85; bys- 
soides, 81; icmadophilus, 81, 85; 
roseus, 81 

Bailey, W. W., 51 

Balsaminaceae, 244 

Baptisia tinctoria, 188 

Barbour, W. C., 135 

Barnhart, J. H., 20, 70, 131 

Basidiomycetes, 211 

Batsodendron arboreum, 153 

Beitrage zur Kenntnis der Hymeno- 
mycetes, II. (Review), 33 

Benedict, R. C., 134 

Berberidaceae, 241 

Bergson and the biometrical method, 68 

Berry, W. E., 200; Additions to the 
Pleistocene Flora of the Southern 
States, 159; Two new Tertiary Species 
of Trapa, 105 

Bessey, C. E., 72 

Betulaceae, 238 

Betula alba papyrifera, 194; lutea, 61, 
183, 184; nigra, I51I, 162; populifolia, 
181, 189, 190 

Biatora anthrocophila, 89; campestris, 
89; chlorantha, 89; chlorosticta, 89; 
cuprea, 89; cupreo-rosella, 89; de- 
colorans, 91; denigrata, 91; exigua, 
89; fossarum, 90; fusco-rubella, 91; 
geophana, 89; granulosa, 89; hyp- 
nophila, 89; icteria, 89; inundata, 90; 
mixta, 90; nigra, 91; parvifolia, 90; 
Resinae, 90; rubella, 90; rufo-nigra, 
‘90; russula, 90; Russellii, 90; sangui- 
neo-atra, 90; Schweinitzii, 90; suffusa, 
90; uliginosa, 90; tricolor, 91; umbrina, 
90; varians, 90; vernalis, 90; virides- 
cens, 90 

Biatorella, 74, 87; campestris 89; fos- 
sarum, 90; resinae, 90; simplex, 86 

Biatorina lutea, 89; mixta, 90; russula, 
90; synothea, 91 

Bignoniaceae, 251 

Bilimbia cupria, 89; hypnophila, 89 

Bisby, G. R., 96, 199 

Blackman, V. H. and Paine, G. S. A 
Recording Transpirometer. (Re- 
view), 128 

Blakeslee, A. F., 135; A Possible Habit 
Mutant of the Sugar Maple (Acer 
Saccharum), 140 

Blastema ferrugineum, 83; ferrugineum 
nigrescens, 83; rupestris, 83 

Boodlea, 6 

Bornetiana, 5 

Boraginaceae, 249 

Bose jC. 255 


Botanic Garden of Grinnel College, 148 

Botanical Magazine, 9 

Botrychium virginianum, 179 

Bouteloua, 58 

Boysia, 137 

Brachyelytrum erectum, 179 

Brackett, M., 69 

Bragg, L., 70 

Brannon, M. A., 95 

Breweria humistrata, 153 

Britton, E. G., 17, 50, 72, 134; Mosses 
of the Virgin Islands and Central 
America, 17 

Britton, E. G., and Williams, 
Central American Mosses, 24 

Britton, N. L., 15, 50, 69, 112, 113, 148, 
‘164, 255; On Erigeron pusillus Nutt., 
197; Selden’s Everyman’s Garden 
Every Week (Review), 128 

Britton, R. H., 148 

Broadhurst, 20, 69, 70, 72, 135; Bergson 
and the biometrical method, 68; 
Winter Changes in Weeping Willow, 
31 

Brooklyn Botanic Garden, 227 

Brown, S., I13 

Bryobesia, 7 

Buchloe, 58 

Buellia dialyta, 83; Elizae, 83; lactea, 
83; myriocarpa, 83; parasema, 83; 
petraea, 83, 169; petraea Montagnei, 
83; pullata, 83; Schraerei, 83; spuria, 
83; stellulata, 83; vernicorna, 83 

Buelliaceae, 83 

Bulletin of the Torrey Botanical Club, 
41 

Burgess, E., 69 

Burlingham, G. S., 134 

Burnham, S. H., and Latham, R. A. 
The Flora of the town of Southold, 
Long Island and Gardiner’s Island, 
201, 229 


R. S. 


Cactaceae, 246 

Caesalpiniaceae, 243 

Caldwell, J. S., 199 

Caliciaceae, 93 

Calicium, 78; byssacaum, 93; Curtisii, 
94; curtum, 94; fuscipes, 94; phaeo- 

. cephalum, 94; parieturnum, 94; ros- 
cidum, 94; roscidum roscidilum, 94; 
subtile, 94; tigillare, 93; tubaeforme, 
94 

Callicostella Oerstediana, 29; pallida, 29 

Callithamnion Baileyi, 99 

Callitrichaceae, 245 

Calman, A., 69 

Caloplaca aurantiaca, 83; aurantiaca 
erytheilum, 84; cinnabarina, 84 

Caloplacaceae, 83 


258 


Campanula dubia, 46; petiolata, 46; 
rotundifolia, 46, 171 

Campanula rotundifolia, Some corolla 
forms of, 46 

Campanulaceae, 252 

Campylopus filifolius, 24; 
gaster, 24 

Candelaria concolor, 85 

Candelariella vitellinum, 85 

Cannabinaceae, 238 

Caprifoliaceae, 251 

Carex, 125; arkansana, 125; conjuncta, 
126; cryptolepis, 157; flava, 155, 156; 
flava androgyna, 156; flava elatior, 
I56, 157; flava graminis, 156, 157; 
flava lepidocarpa, 156; flava recti- 
rostra, 156, 157; lepidocarpa, 155- 
I57; lepidocarpa laxior; Oklahomen- 
sis, 126; Muhlenbergii, 189; penn- 
sylvanica, 173; stipata, 125, 126; 
virescens, 177; vulpina, 125 

Carpinus caroliniana, 178 

Carya alba, 175; glabra, 174, 175; ovata, 
175 

Caryophyllaceae, 240 

Cassiatae, III 

Cassiope tetragona, 65 

Castanea, 176, 178 

Caulerpa, 7, 8 

Caulophyllum thalictroides, 183 

Ceanothus americanus, 173, 191 

Celastraceae, 245 

Celastrus scandens, 183 

Centaurea, 160 

Central American Mosses, 24 

Cephalanthus occidentalis, 151 

Ceramium rubrum, 98, 101 

Cerastium arvense, 173 

Ceratodon purpureus, 170, 171 

Cetraria aleurites, 85; aurescens, 84; 
ciliaris, 84; Fahlunensis, 84; Fendleri, 
84; glauca 84; Islandica, 84; juniper- 
ina, 84; juniperina Pinastri, 84; lacu- 
nosa, 84; Oakesiana, 84; placorodia, 
85 

Chaenotheca, 93; phaeocephala, 94 

Chaetochloa sp., 160 

Chaetomorpha, 99; Linum, 99 

Chairmen of Special Committees on 
Local Flora, Torrey Botanical Club, 
134 

Chamberlain, }., death of, 132 

Chamaesyce, 227 

Chamaecyparis nootkatensis, 61; thy- 
oides, 56 

Champia, 99; parvula, 100 

Characeae, 225 

Chase, A., 19 

Chenactis Nevii, 19 

Chenopodiaceae, 239 


subleuco- 


Chimaphila umbellata, 61, 177 

Chondrophora virgata, 154 

Chondrus crispus, 98, 100 

Cichoriaceae, 252 

Chrysanthemum integrifolium, 66 

Cistaceae, 246 

Cladonia alpestris, 80; alpicola Karelica, 
81; bellidiflora, 80; Botryella, 81; 
caespiticia, 81; cariosa, 81; coccifera, 
80; cornucopioides, 80; cornuta, 81; 
crispata, 81; cristatella, 80; cristatella 
ochrocarpia, 80; decortica, 81; delica, 
81; degenerans, 81; fimbriata ad- 
spersa, 80; fimbriata tubaeformis, 81; 
fimbriata simplex, 81; furcata, 80; 
170; furcata crispata, 81; furcata 
racemosa, 80; furcata subulata, 80; 
gracilis elongata, 81; graciles hybrida, 
81; graciles symphiacarpa, 81; graciles 
verticillata, 81; lepidata, 80; maci- 
lenta, 80; mitrula, 81; palamaea, 80; 
papillaria, 80, 188; pyxidata, 81, 170; 
pyxidata symphicarpia, 81; rangi- 
ferina, 170; rangiferina alpestris, 80; 
rangiferina sylvatica, 80; sylvatica, 
80, 170, 188; squamosa, 81; squamosa 
delicata, 81; subcariosa, 81; turgida, 
81; uncialis, 80, 170; uncialis adunca, 
80; verticillata, 81 

Cladoniaceae, 80 

Cladoniei, 80 

Cladophora, 6 

Cladophoris, 6 

Clapp, G. L., 199 

Clad 3D» 20570) 

Classification of Botanical Science in 
Two Dimensions, A, 144 

Clavariaceae, 214 

Clerodendrum indicum, 23; infortunata, 
23; Siphonanthus, 23; spinosum, 23 

Clethraceae, 247 

Clintonia, 61 

Cochlearia groenlandica, 66 

Cockerell, T. D. A., Two New Plants 
from the Tertiary Rocks of the West, 
135 : 

Coleosporiaceae, 211 

Coleogyne ramosissima, 64 

Collema cyrtaspis, 92; floccidum, 92; 
furvum, 92; leptaleum, 92; micro- 
phyllum, 92; myricoccum, 92; molyb- 
dium, 87; molybdium cronia, 88; 
nigrescens, 92; nigrescens leucopepla, 
92; plicata, 93; pulposum, 92; pyc- 
nocarpum, 92; ryssoleum, 92; tenax, 
92; verruciforme, 92; vespertilio, 92 

Collemaceae, 92 

Collinsonia canadensis, 179 

Comandra umbellata, 173 

Commelinaceae, 235 


Compositae, 252 

Coniferous Forests of Eastern North 
America, 70 

Coniocarpineae, 93 

Connecticut, The Vegetation of, 167 

Conotrema urceolatum, 91 

Convallariaceae, 236 

Convolvulaceae, 249 

Cook, M. T., 50, 135; Les Zoocécidies 
des Plantes d’Europe et du Bassin de 
la Méditerranée (Review), 32 

Copake Falls, N. Y., 1913 Notes on the 
Flora of, 42 

Coprinus nychtemerus, 34 

Corallina officinalis, 101 

Corallorrhiza maculata, 179 

Corema Conradii, 56 

Cornaceae, 247 

Cornus canadensis, 61; circinata, 183; 
florida, 61, 176, 179; Nuttallii, 61 

Corydalis sempervirens, 171 

Corylus americana, 177, I91 

Cowell, J. F., 50 

Crassulaceae, 242 

Crataegus, 37 

Crootheca Richteriana, 196 

Crouch, G. S., 38 

Cruciferae, 241 

Cryphiacanthus angustifolius, 21 

Cucurbita Pepo, 34 

Cupressus macrocarpa, 63 

Current Literature and Notes, 32 

Cuscutaceae, 249 

Cyclocarpineae, 78 

Cyperaceae, 233 

Cyperus filiculmis macilentus, 189 

Cyphelium tigillare, 93 

Cypripedium acaule, 43, 177; passeri- 
num, 65; parviflorum pubescens, 43 

Cypselea, 68 

Cystoclonium purpurascens, 98, 99 


Dacryomycetaceae, 213 

Danthonia spicata, 171 

Dasya elegans, 5; pedicillata, 5 

Davis, J. J., Occurrence of Indian Pipe, 
162 

Delesseria sinuosa, 100 

De Merritt, M., 199 

Dentriscocaulon bolacinum, 93 

Dermatocarpaceae, 94 

Dermatocarpon arboreus, 94; fluviatile, 
94; hepaticum, 94; miniatum, 95; 
170; miniatum complicatum, 95; 
rufescens, 95 

Dermatolithon pustulatum, 100 

Desmarestia aculeata, 98, 99; viridis, 
I00 

Desmodium canadense, 189; sp., 177 

Dianthera, 150; americana, I51I, 154 


9 


oa 


59 


Dicentra cucullaria, 183 
Dichodium byssinum, 88 
Dicotyledones, 237 
Dicranum scoparium, 171 


-Dictyosphaeria, 6 


Diels, L., 53 

Dinkelspiel, Mrs. H., 69 

Dioscoreaceae, 236 

Diplochistes scruposus, 91 

Diptochistaceae, 91 

Dodses BO.) 120, 70; 1307) 134th 5 
Proceedings of the Club, 11, 17, 70, 
130, 131, 163-165 

Draba glacialis, 66; hirta, 65 

Droseraceae, 242 

Dryas integrifolia, 66 


Eakins, Mrs. P., 69 

East, E., 53 

Echinopanax horridum, 61 

Ectropothecium apiculatum, 30; globi- 
theca, 30; pseudo-rutilans, 30 

Edible Fungi, 163 

Egglestch, W. W., 113 

Eleocharis mutata, I51I, 153 

Endocarpon arboreum, 94; hepaticum, 
95; miniatum, 95; miniatum aqua- 
tium, 95; miniatum complicatum, 95; 
rufescens, 95 

Endothia gyrosa parasitica, 180 

Engler, A., 95 

Entodon stenocarpus, 26 

Ephebaceae, 93 

Ephebe lanata, 93; pubescens, 93 

Ephedra, 64 

Epifagus virginiana, 179 

Epigaea repens, 177 

Epilithon membranaceum, ror 

Epilobium angustifolium, 181 

Epipactis pubescens, 179 

Equisetaceae, 230 

Eragrostis pectinacea, 189 

Erechtites hieracifolia, 181 

Ericaceae, 247 

Eriocaulaceae, 235 

Erigeron canadensis, 181, 189, 197, 198; 
pusillus, 197 

Esther Herman Fund, 70 

Euhomalia, 28 

Eumycetes, 206 

Euphorbia campestris, 137 

Euphorbiaceae, 245 

Euphyceae, 204 

Euthallophyta, 204 

Evans, A. W., 20, 70, 134 

Evening Post, 20, 51, 53, 199 

Evernia furfuracea, 79; furfuracea 
Cladonia, 79; prunastri, 79; meso- 
morpha, 140 

Exobasidiaceae, 213 


260 


Fabaceae, 243 

Fabatae, III 

Fabronia flavinervis, 27; polycarpa, 27 

Fagaceae, 238 

Fagus americana, 162; grandifolia, 57, 
178 

Fisher, G. C., 17, 51 

Flora of the Town of Southold, Long 
Island and Gardiner’s Island, The, 


201, 229 

Fragaria virginiana, 189 

Franseria, 13-15; acanthicarpa, 13; 
Bryanti, I4; eriocentra, 14; tenui- 
folia, 13 

Fraxinus americana, 178; caroliniana, 
153 


Fromme, F. D., 38 
Fulton, H. R., 38 

Funaria hygrometrica, 192 
Fungi, 206 


Gaertneria, 13, 14 

Gager, C. S., Gibson’s Supplement to 
Jost’s Plant Physiology (Review), 109 

Garden and Forest, 72 ° 

Gardener’s Chronicle, 9 

Gasteromycetes, 218 

Gastrodonta, 137 

Gates, R. R., 199 

Gaultheria procumbens, 177; Shallon, 61 

Gaylussacia baccata, 173, 177 

Geaster, 104 

_Gentiana Andrewsii, 108; asclepiadea, 
108; quinquefolia, 43, 44, 108 

Gentianaceae, 248 

Geocarpon, 67; minimum, 67 

Geraniaceae, 244 

Geranium maculatum, 
anum, 183 

Gerard, W. R., death of, 71 

Gerardia flava, 177 

Gibson’s Supplement to Jost’s Plant 
Physiology (Review), 109 

Gleason, H. A., 113 

Gleocapsa aeruginosa, 196; gelatinosa, 
196; quarternata, 196; violacea, 196 

Gleotheca linearis, 196 

Goldfussia glomerata, 35 

Gortner, R. A., 131 

Gow, J. E., death of, 199 

Gramineae, 231 

Graphidaceae, 91 

Graphis, 78; dendritica, 91; elegans, 91; 
erumpens, 9I; scripta, 91; scripta 
assimilis, 91; scripta graciliens, 91; 
scripta recta, 91; sculpturata, 91 

Graves, A. H., 227 

Griffithsia, 5 

Grimmia Olneyi, 170 

Grossulariaceae, 242 


177; Roberti- 


Gundersen, A. L., 199 

Gymnocarpales, 78 

Gymnocarpi, 78 . 

Gymnogongrus Torreyi, 99 

Gymnospermae, 230 

Gyrophora Dilleni, 88; ee 
88; vellea, 88 

Gute emcee 88 

Gyrostomum urceolatum, 91 


Habenaria hyperborea, 45 

Halimeda, 6 

Halothrix lumbricalis, 100 

Haloragidaceae, 247 

Hamamelidaceae, 242 

Hamamelis virginiana, 179 

Harper, R. A.,/17, £8, 20; 60; 70mazoy 
134, 148; Proposed Work on the Cryp- 
togamic Flora of the Region About 
New York, 133; Spore Formation in 
the Slime Moulds, 17 

Harper, R. M., 16, 70, 148; The Aquatic 
Vegetation of Squaw Shoals, Tusca- 
loosa County, Alabama, 149; A Clas- 
sification of Botanical Science in Two 
Dimensions, 144 

Harperella fluviatilis, 151-154 

Harper’s Report on Forests of Alabama 
(Review), 47 

Harpophyllum aureum, 29 

Harris, J. A., 20, 70, 131, 255. 

Harrison, R. G., 96 

Harshberger, J. W., 132; Algal Stalac- 
tites in Bermuda, 195 

Haynes, C. C., 130 

Hazen, T. E., 134 

Hedwigia ciliata, 170 

Hedysarum Mackenzii, 65 

Helianthemum majus, 188 

Helianthus divaricatus, 173, 174 

Helicophyllum torquatum, 29 

Hemiambrosia, 14, 

Hemixanthidium, 14 

Henry, J. K., A New Form of Pyrola 
bracteata, 32; Two British Columbian 

- Notes, 45 

Hepatica triloba, 177 

Hepaticae, 223 

Heppia Despreauxii, 93; virescens, 93 

Heppiaceae, 93 

Herpyzonema, 7 


Hess, G. W., 20 
Heterothecium pezizoideum, 91; vul- 
pinum, 91 


Hicoria aquatica, 161, 162; sp., 57 

Hieracium, 37; venosum, 177 

Hill, E. J., Whorled leaves in Gentiana, 
108 

Hollick, A., 19, 148 

Holmes, W., 69 


9) 


° a 


Holtze, N., 38 

Homalia, 28, 29; glabella, 29; lentula, 
28; membranacea, 28 

Hookeria membranacea, 28 

House, H. D., Violets New to South- 
western Virginia, 2 

Howe, M. A., 18, 20, 70, 131, 134, 165, 
255; Some Midwinter Algae of Long 
Island Sound, 97; Two Recent Works 
on the Marine Algae (Review), 4 

Howe, R. H., Jr., Some Comparisons of 
the Lichen Floras of Eurasia and 
North America, 138 

Hull, E. D., 131; Occurrence of the 
Indian Pipe (Monotropa uniflora) in 
a Xerophytic Habitat, 1o1 

Humphreys, E. W., Some Fossil Leaves 
and their Significance, 39 

Hydnaceae, 214 

Hydotheria venosa, 88 

Hymenocallis coronaria, I5I, 153}; oc- 
cidentalis, 152 

Hymenoclea, 15 

Hymenostomum Breutelii, 18 

Hyophila, 18; reflexifolia, 25 

Hypericaceae, 246 

Hypericum galioides, 151; gentianoides, 
188; perforatum, 45; punctatum, 45 

Hypopterygium Tamarisci, 29 

Hypomycetes, 209 


Icmadophila ericetorum, 81, 85 

Ilea, 7 

Ilicaceae, 245 

Index Filicum, 37 

Index Kewensis, 37 

Influence of Calcium, Magnesium and 
Potassium Nitrates upon the Toxicity 
of Certain Heavy Metals toward 
Fungus Spores (Review), 33 

Influence of Preceding Seasons on the 
Growths of Yellow Pine, The, 115 

Insect Galls, 203 

International Phytogeographical Ex- 
cursion in America, The, 55 

International Phytogeographical 
cursion of 1913, The, 129 

Iridaceae, 236 

Iris versicolor, 43 

Isodrepanium, 18, 27, 28; lentulum, 27, 
28 

Isopterygium miradoricum, 30; pusil- 
lum, 30; trichopelma, 30 

Itea virginica, 151 


Ex- 


Jolivette, H. D. M., 255 
Journal of Heredity, The, 11 
Juglandaceae, 237 

Juglans cinerea, 184 
Juncaceae, 235 


61 


Juniperus communis, 189, 193; mono- 
sperma, 64; scopulorum, 58; virgini- 
ana, 173, 193 


Kaliella turbinata, 197 

Kalmia angustifolia, 189; latifolia, 153, 
177, 179 

Keeler, Mrs. L. M., 69 

Kennedy, P. B., 19 

Kern, F. D., 38 

Kew Bulletin, 38, 112 

King, C. A., 135 

Kirkwood, J. E., The Influence of Pre- 
ceding Seasons on the Growth of 
Yellow Pine, 115 

Kochia, 60 

Krigia virginica, 43, 171 

Kunkel, L. O., 16; The Influence of 
Calcium, Magnesium and Potassium 
Nitrates upon the Toxicity of certain 
Heavy Metals toward Fungus Spores 
(Review), 33 


Labiatae, 249 

Labiduromma bormansi, 135 

Laminaria, 99; Agardhii, 98; digitata, 98 

Larix laricina, 57 

Latham, M. E., 135 

Latham, R. A., & Burnham, S. H., The 
Flora of the Town of Southold, Long 
Island and Gardiner’s Island, 201, 229 

Lauraceae, 241 

Lawrence, J. V., 131 

Lecanora, 87; atra, 86; allophana, 86; 
athroocarpa, 86; albella cancriformis, 
86; Bockii, 86; cervina, 86; cervina 
discreta, 86; cinerea, 86, 169; Cu- 
pressi, 86; fuscata, 85; gibbosa, 86; 
Hageni, 86; lacustris, 86; muralis, 86; 
orosthea, 86; pallescens, 86; pallida, 
86; pallida cancriformis, 86; privigna, 
86; rubina, 86; subfusca, 86; subfusca 
distans, 86; symmicta, 86; tartarea, 
86; varia, 86; varia saepincola, 86; 
Willeyi, 86; xanthophana, 86 

Lecanoraceae, 85 

Lechea tenuifolia, 171 

Lecidia alba, 89; albocoerulescens, 89; 
anthracophila, 89; athroocarpa, 86; 
contigua, 88; cuprea, 89; deco’orans, 
91; elaeochroma, 89; enteroleuca, 88; 
granosa, 88; granulosa, 89; lutea, 89; 
muscorum, 89; parasema, 83; para- 
sema elaeochroma, 89; parvifolia, 90; 
rufo-nigra, 90; spilota, 89; tessellata, 
89; tessellina, 88; uliginosa, 90; va- 
rians, 90; vernalis, 90; viridescens, 90 

Lecidiaceae, 88 

Ledum decumbens, 66 

Lemnaceae, 235 


262 - 


Lentibulariaceae, 250 
Lepidopilum, 27, 28: membranaceum, 28 
Lepthorapsis derinidis, 94 
Leptilon canadense, 199; pusillum, 198 
Leptogium bolacinum, 93; chloromelum, 
. 93; dactyinum, 093; lacerum, 93; 
microphyllum, 92; myccochorum sa- 
turinum, 93; palmatum, 93; plicatile, 
93; pulchellum, 93; saturinum, 93; 
scotinum, 93; tenuissimum, 93; tre- 
melloides, 93 
Leskea microcarpa, 3! 
Lespedeza capitata, 173, 188; Nuttallii, 
173 
Les Zoocécidies des plants d’Europe et 
du Bassin de la Méditerranée (Re- 
view), 32 
Letharia, 139; columbiana, 139; tham- 
nodes, 79, 140; vulpina, 139; vulpina 
californica, 139 
Leucobryum antillarum, 25; glaucum, 
yl, 17/2 
Levine, M., 135; Beitrage zur Kenntnis 
der Hymenomyceten, II (Review), 
33; Proceedings of the Club, 17, 40, 
69, 120, 130, 163 
Liatris scariosa, 173 
Libocedrus decurrens, 63 
Lichens, 219 
Lichina.confinis, 93 
Lichinaceae, 93 
Liliaceae, 236 
Linaceae, 244 
Linnaea borealis, 61 
Liquidambar styraciflua, 151 
Liriodendron Tulipifera, 178 
List of Plants Collected on the Stefan- 
son-Anderson Arctic Exploration, 
I9Q08-12, 65 
WLobaria, 87; amplissima, 87; pulmon- 
aria, 87; quercizans, 87 
-Lobeliaceae, 252 
-Long Island Historical Society, 227 
-Long Island Sound, Some Midwinter 
Algae of, 97 
iLopadium pezizoideum, 91; vulpinum, 
QI 
‘Louisiana, Two Additions to the Flora 
of, 21 
Lupinus arcticus, 65, 66; perennis, 43, 
102, 189 
Lutz, F. E., 50 
Lycoperdon, 104 
Lycopodiaceae, 230 
Lycopodium lucidulum, 61, 179 
Lysimachia quadrifolia, 177, 189 
iLythraceae, 246 


Macbride, T. H., 132 
Mackenzie, K. K., A New Genus from 


Missouri, 67; A New Northeastern 
Sedge, 155; A New Southwestern 
Sedge, 125 

Macmillan, H. F., 38 

Macromitrium, 18; palmense, 25; sub- 

cirrhosum, 25, 26; Tonduzii, 25 

Magazine San Diego, 132 

Magnoliaceae, 240 

Maianthemum, 61; canadense, 177 

Mairania alpina, 66 

Malaceae, 243 

Malvaceae, 245 

Mansfield, W., 18, 20, 69, 70 

Maronea constans, 83 

Marquette, W. G., Blackman, V. H. & 
Paine, S. G. A Recording Trans- 
spirometer (Review), 128; Ueber den 
Einfluss des Tabakrauches auf der 
Pflanze (Review), 34; Wager, H. 
The Action of Light on Chlorophyll 
(Review), 111; Warner, C. H. For- 
maldehyde as an Oxidation Product 
of Chlorophyll Extracts (Review), I1I 

McDermott, F. A., Tri- and Tetra- 

carpellary Walnuts, 127 

Medeola virginiana, 179 

Melampsoraceae, 211 

Melampyrum lineare, 177 

Melanconiales, 209 

Melanthaceae, 236 

Melastomaceae, 246 

Melobesia Lejolisii, 100 

Mendelian Society of Vienna, 53 

Menyanthes trifoliata, 43 

Mesospora, 8 

Metcalf, H., 38 

Microcystis flos-aqua; 196 

Microdictyon, 6 

Milanotheca cruenta, 94 

Minns, S., 131 

Missouri Botanical Garden, 165 

Missouri, A New Genus from, 67 

Mitchella repens, 177 

Mittenothamnium Langsdorfi, 30; me-. 
gapalmatum, 30; nicaraguense, 30; 
reptans, 30; Salleanum, 30; sub- 
striatum, 30 

Mnium Nevii, 19 © 

Monascus, 47 

Monocotyledones, 230 

Monotropa uniflora, 101, 179 

Monotripliceae, 247 

Moraceae, 238 

Mosses of the Virgin Islands and Central 
America, 17 

Murrill, W. A., 17, 18, 134, 163 

Musci, 223 

Mycologia, 164 

Mycoporaceae, 94 

Mycoporum pycnocarpum, 94. 


263 


Myricaceae, 237 

Myrica asplenifolia, 173, 181, 188, 191; 
carolinensis, 188, 189 

Myxomycetes, 204 

Myxothallophyta, 204 


Naturalists’ Directory, 200 

Nature, 38 

Nature and Inheritance of Fasciation, 

, 1 : 

Neckera, 28; Ehrenbergii, 26; falcifolia, 
28; lentula, 28 

Negundo, 41; triloba, 40, 42 

Nephroma Helveticum, 87; laevigatum, 
87; tomentosum, 87 

Nephromopsis ciliaris, 84 

Nevius, R. D., death of, 19 

Nevinsia alabamensis, 19 

New Form of Pyrola bracteata, A, 32 

New Genus from Missouri, A, 67 

New Northeastern Sedge, A, 155 

New Southwestern Sedge, A, 125 

News Items, 18, 37, 50, 71, 95, 112, 131, 
148, 165, 190, 227 

New York Botanical Garden, I12; 
Meetings at, 11, 17, 70, 130, 163, 164 

Nichols, G. E., 129; The International 
Phytogeographic Excursion in Ameri- 
ca, 55; The Vegetation of Connecticut 
—III, 167 

Nineteen thirteen (1913) Notes on the 
Flora of Copake Falls, N. Y., 42 

Nymphaeaceae, 240 

Notes on the Local Flora, 131 


Occurrence of Indian Pipe, 162 

Occurrence of the Indian Pipe (Mono- 
tropa uniflora) in a Xerophytic Habi- 
tat, IO 

Observations on Sphaerosoma and allied 
Genera, 164 

Ochrolechia pallescens, 86; tartarea, 86 

Oenothera biennis, 188 

Oleaceae, 248 

Olive, E. W., 135; Steven’s Fungi which 
Cause Plant Diseases (Review). 46 

On Erigeron pusillus Nutt., 197 

Onagraceae, 246 

Opegrapha rimalis, 92; varia, 92; viridis, 
92; vulgata, 92 

Ophioglossaceae, 229 

Opuntia Rafinesquii, 102; vulgaris, 171 

Orchidaceae, 236 

Oreohelix, 137 

Orobanchaceae, 250 

Orthostichidium pentagonum, 26 

Origin and Development of Lamellae in 
Coprinus micaceus, The, 165 

Osmunda regalis, 151 

Osmundaceae, 229 


Ostrya virginiana, 176, 179 
Ovieda mitis, 22; spinosa, 23 
Oxalidaceae, 244 

Oxalis, 61 

Oxyria digyna, 66 


Pachynae, 139 

Paleobotanischen Zentralblatt, 200 

Panicum dichotomum, 177; depauper- 
atum, 189; virgatum, 150, I5I, 154 

Pannaria byssina, 88; languinosa, 88; 
leucosticta, 88; lurida, 88; micro- 
phylla, 88; molybdaea, 87; molyb- 
daea cronia, 88; nigra, 88; rubiginosa, 
88; tryptophylla, 87 

Pannariaceae, 87 

Papaver radicatum, 66 

Papaveraceae, 241 

Papillaria nigrescens, 26 

Parmelia Aleurites, 85; 
Borreri rudecta, 85; caesia, 84; 
caperata, 85, 170; centrifuga, 85; 
cetrata, 84; conspersa, 85, 170, 172; 
crinita, 84; furfuracea, 79; furfuracea 
Cladonia, 79; laevigata, 84; olivacea, 
85; olivaria, 85; perforata, 85; perlata, 
85; pertusa, 84; physodes, 85; saxi- 
talis, 85; saxitalis sulcata, 85; tiliacea, 
85 

Parmeliaceae, 84 

Parmeliella tryptophylla, 87 

Parmeliopsis aleurites, 85; ambigua, 85; 
placorodia, 85 

Parsons, T. H., 38 

Peach Yellows and Methods of their 
Control, 50 

Pedicularis arctica, 66; canadensis, 177; 
lanata, 66 

Peltigera apthosa, 87; canina, 87; 
canina spuria, 87; horizontalis, 87; 
polydactyla, 87; rufescens, 87; spuria, 
87; venosa, 87 

Peltigeraceae, 87 

Persia pubescens, 161 

Pertusaria communis, 87; globularis, 86; 
glomerata, 87; leioplaca, 87; multi- 
puncta, 86; pustulata, 87; velata, 87; 
Wulfenii, 87 i 

Pertusariaceae, 87 

Petalonia, 8 

Phaeographis dendritica, 91 

Phascum, 18 

Phegopteris polypodioides, 179 

Phellorina, 17 

Philonotis sphaerocarpa, 26; uncinata 
gracilenta, 26 

Phlox pilosa, 102; Richardsonii, 66 

Phormidium laminosum, 196 

Phrymaceae, 251 

Phycomycetes, 206 


Borreri, 85; 


264 


Phyllitis, 5, 7, 8 

Phyllogonium fulgens gracile, 26; vis- 
cosum, 26 

Phyllophora membranifolia, 100; Bro- 
diaei, 100, 101 

Physcia adglutinata, 82; aquila, 82; 
aquila detonsa, 82; detonsa, 82; 
caesia, 84; hispida, 82; hypoleuca, 82; 
obscura, 82; obscura endochrysea. 82; 
obscura endococcina, 82; pulveru- 
lenta, 82; speciosa, 82; speciosa galac- 
tophylla, 82; stellaris, 82; tenella, 82; 
tribacea, 82, 169 

Physiaceae, 82 

Physcomitrium turbinatum, 192 

Physma lurida, 88 

Phytolacca decandra, 151, 181 

Phytolaccaceae, 240 

Picea Engelmanni, 59 

Pickett, F. L., 60 

Pilotrichum bipinnatum, 27 

Pinaceae, 230 

Pinus, 160; aristata, 60; edulis, 58, 64; 
flexilis, 59; Lambertiana, 62, 63; 
Murrayana, 63; ponderosa, 62-64, 
I16-119; ponderosa scopulorum, 58, 
59; rigida, 56, 189; Sabiniana, 63; 
Strobus, 175, 194 

Pisum, 34 

Placodium aurantiacum, 83; auran- 
tiacum erythellum, 84; cerinum, 83; 
cinnabarinum, 84; ferrugineum, 83; 
rupestre, 83; vitellinum, 85 

Placythium nigrum, 88 

Placyrthium, 88 

Plant Breeding in Scandinavia (Re- 
view), 35 

Plant Societies on Uplands, 167 

Plantae Wilsonianae, 9 

Plantaginaceae, 251 

Platanaceae, 242 

Platanus occidentalis, 151, 161 

Platysma aurescens, 84; Fendleri, 84; 
glaucum, 84; Islandica, 84; juniperina, 
84; juniperina Pinastri, 84; lacunosa 
Atlanticum, 84; lepatizon, 84; Oakesi- 
anum, 84 

Plumbaginaceae, 248 

Pneumaria maritima, 66 

Poa compressa, 171, 172, 189; pratensis, 
173 

Podaxon, 17 

Podostemon, I51 

Pohlia falcata, 26 

Polemoniaceae, 249 

Polyblastea lactea, 83 

Polyblastiopsis lactea, 94 

Polygala paucifolia, 43 

Polygalaceae, 244 

Polygonaceae, 238 


Polygonatum biflorum, 179 

Polygonella articulata, 188 

Polygonum fugax, 66; sp., 160 

Polypodiaceae, 229 

Polypodium vulgare, 173 

Polyporaceae, 215 

Polysiphonia elongata, 99, 100; ni- 
grescens, 101; urceolata formosa, TOT 

Polystichum acrostichoides, 177 

Polytrichum antillarum, 26; commune, 
I79; juniperinum, 171; piliferum, 171, 
188; vernicosum, 26 

Pontederiaceae, 235 

Pool, R. J., 72 

Popper, Mrs. A., 69 

Populus deltoides, 160; grandidentata, 
I8I, 193; temuloides, 181, 193 

Poronia faginea, 94 

Porotrichum sp., 26 

Portulacaceae, 240 

Possible Habit Mutant of the Sugar 
Maple (Acer saccharum), A, 140 

Potentilla argentea, 171; canadensis, 
189; pulchella, 66 

Prain' 2D 8 

Preliminary List of the Lichens found 
within a Radius of 100 Miles of New 
York City, 73 

Proceedings of the Club, 11, 49, 69, 70, 
129, 163 

Primula borealis, 66 

Primulaceae, 248 

Proposed Work on the Cryptogamic 
Flora of the Region About New Yerk, 
133 

Protoboysia, 137 E 

Prunus corymbulosa, 65; serotina, 178; 
virginiana, 173, I81 

Psedera quinquefolia, 183 

Pseudophyscia aquila, 82; aquila de- 
tonsa, 82; comosa, 82; hypoleuca, 82; 
speciosa, 82; speciosa galactophylla, 
82 

Pseudophyciaceae, 82 

Pseudotsuga, 63, 64; taxifolia, 59, 60, 
I24 f 

Psora icteria, 89; Russellii, 90 

Psorotichia Schaereri, 93 

Pteridophyta, 229 

Pterigonidium pulchellum, 31 

Pteris aquilina, 102, 103, 173, 177, 189 

Puccinia graminis, 47 

Pucciniaceae, 211 

Punctaria latifolia, 100 

Pycnanthemum virginianum, 173 

Pylaiella littoralis, ror 

Pyramidula, 137 

Pyrenopsidaceae, 93 

Pyrenopsis Schroederi, 93 

Pyrenula cinchonae, 94; hylaspora, 94; 


265 


lactea, 94; leucoplaca, 94; nitida, 94; 
95; pachycheila, 94; punctiformis, 94; 
thelaena, 94 

Pyrenulaceae, 94 

Pyrenocarpales, 94 

Pyrola americana, 177; aphylla, 32; 
aphylla paucifolia, 32; bracteata, 32; 
bracteata Hillii, 32; elliptica, 177 

Pyrolaceae, 247 

Pyxine cocoes, 82; sorediata, 82 


‘Quercus alba, 175, 176, 178; californica, 
62; coccinea, 175; Garryana, 62; 
Gunnisonii, 58; heterophylla, 132; 
ilicifolia, 173, 191; marilandica, 56; 
phellos, 161, 162; pridigitata, 162; 
Prinus, 175; prinoides, 173; rubra, 
176, 178; Rudkini, 132; sp., 57; stel- 
lata, 174, 173; velutina, IOI, 102, 175, 
187; virginiana, 161 


Racomitrium Nevii, 19 

Radiatae, 78 

Radiati-Stratosi, 80 

Ramalina, 140; calicaris, 79, 140; 
calicaris canaliculata, 79; calicaris 
farinacea, 79; calicaris fastigata, 79; 
calicaris fraxinea, 79; candiculata, 79; 
Duriaei, 140; farinaceae, 79; fastigi- 
ata, 79; fastigiata subampliata, 79; 
fraxinea, 140; Mensiezii, 140; rigida, 
79; scopulorum, 140; subfarinacea, 
I40; Urlleyi, 79 

ands ys Vi, 70 

Ranunculaceae, 240 

Ranunculus nivalis, 66 

Record, S. J., Harper’s Report on Forests 
of Alabama (Review), 47 

Reichling, G. A., 164 

Reviews, 4, 46, 109, 128, 226 

Reynolds, C. L., 20 

Rhacopilum angustatum, 29; latistip- 
ulatum, 29; tomentosum, 29; tomen- 
tosum longe-aristatum, 29 

Rhamnaceae, 245 

Rhizocarpon petraea, 83 

Rhizoclonium, 6 

Rhizogonium spiniforme, 26 

Rhododendron albiflorum, 45; albi- 
florum poikilon, 46; catawbiense, 154; 
lapponicum, 65; nudiflorum, 177 

Rhododermis Georgii, Ior 

Rhodomela subfusca, 101 

Rhodora, 197 

Rhodymenia palmata, 99 

Rhus, 39, 40; copallina, 40, 173; glabra, 
39, 40, 42, 191; hirta, 173; Powelliana, 
39, 40; typhina, 172, 174; Tox.:co- 
dendron, 183, 189; Uddeni, 39, 42 

Richards, H. M., 20, 70, 130, 135 


Rigg, G. B., 199 

Rinodina ascociscana, 83; confragosa» 
83; constans, 83; exigua, 89; sophodes: 
83; spohodes confragosa, 83 

Robinia Pseud-Acacia, 189 

Robinson, C. B., death of, 19, 37, I31 

Rolloff, A., 199 

Rosa, 35; acicularis, 65; humilis, 173 

Rosaceae, 242 

Rubiaceae, 251 

Rubus allegheniensis, 181; ideaus acu- 
leatissimus, 181; odoratus, 183; vil- 
losus, 189 

Ruellia angustifolia, 21, 22; spectabilis, 
21, 22; Tweediana, 21, 22 

Rumex Acetosella, 171, 189 

Rusby, H. H., 12; Addison Brown, 1 

Rydberg, P. A., 12; List of Plants 
Collected on the Stefanson-Anderson 
Arctic Exploration, 1908-12, 65 


Sagedia lactea, 94; oxespora, 94 

Salicaceae, 237 

Salix anglorum, 66; arctica, 65; nigra, 
I51; phlebophylla, 66 

Salton Sea, The (Review), 226 

Sambucus racemosa, 183 

Sanguinaria canadensis, 42 

Sanicula marilandica, 179 

Santalaceae, 238 

Sapindopsis, 40; magnifolia, 40, 42; 
variabilis, 40, 42 

Sapindus, 40, 41; membranaceus, 40, 
42; saponaria, 40, 42 

Sarcobatus, 60 

Sargassum, 6, 8; bacciferum, 8; Filipen- 
dula, 99 

Sarracenia flava, 154 

Sassafras variifolium, 176, 179 

Saxifraga virginiensis, 171 

Saxifragaceae, 242 

Schaffner’s Field Manual of Trees (Re- 
view), IIO 

Schenck, C. A., 51 

Schenzeriaceae, 230 

Schizomycetes, 206 

Schizothrix calcicola, 196 

Schley, E., 199 

SchGéney, L., death of, 51, 130 

Schwendener, S., 72 

Science, 53, 72, 95, 199, 255 

Scirpus americanus, 151 

Scrophulariaceae, 250 

Scytosiphon lomentarius, 98 

Seaver, F. J., 135, 164 

Sedum Nevii, 19 

Selaginella rupestris, 171 

Selaginellaceae, 230 

Selden’s Everyman’s Garden Every 
Week (Review), 128 


266 


Sematophyllum caespitosum, 31; gali- 
pense, 31; Lindigii, 31; microcarpum, 
31; xylophilum, 31 

Sequoia gigantea, 63; sempervirens, 53 

Sericocarpus asteroides, 173, 189 

Shimek, B., 95 

Shorter Notes, 31, 68, 108, 127, 162 

Simaroubaceae, 244 

Siphonanthus indica, 22, 23 

Smilaceae, 236 

Smilacina racemosa, 177 

Smilacites grandifolia, 135 

Smilax, 135, 136; aspera, 136; carbo- 
nensis, 135, 136; grandifolia, 135, 
136; Kansana, 136; labidurommae, 
135; lamarensis, 136; laurifolia, 136; 
lingulata, 136; undulata, 137 

Solanaceae, 250 

Solidago bicolor, 177; caesia, 177; lati- 
folia, 179; nemoralis, 173, 189 

Some Aspects of Californian Coastal 
Vegetation, 130 

Some Comparisons of the Lichen Floras 
of Eurasia and North America, 138 

Some Fossil Leaves and their Signi- 
ficance, 39 

Some Midwinter Algae of Long Island 
Sound, 97, 165 

Sparganiaceae, 230 

Sparganium sp., 160 

Spathularia, 28 

Spermatophyta, 230 

Spermothamnium Turneri, 99 

Sphacelaria cirrhosa, 99 

Sphaeropsideae, 210 

Spore Formation in the Slime Moulds, 
17 

Squamidium macrocarpum, 26 

Standley, P. C., Two Additions to the 
Flora of Louisiana, 21 

Staphylea trifolia, 183 

Staten Island Association of Arts and 
Sciences, 148 

Statice sibirica, 66 

Stenocybe byssacaum, 93 

Stenophyllus capillaris, 188 

Stereocaulon denudatum, 80; paschale, 
80, 170; tomentosum, 80 

Sterrocolax decipiens, 99 

Stetson, S., 69, 134; 1913 Notes on the 
Flora of Copake Falls, N. Y., 42 

Stevens, F. L., 18 

Stevens’ Fungi which Cause Plant 
Diseases (Review), 46 

Sticta amplissima, 87; aurata, 87; 
crocata, 87; pulmonaria, 87; querci- 
zans, 87; sylvatica, 87 

Stictaceae, 87 

Stober, J. B., 199 

Stoddard, E. D., 53 


Stout, A. B., 20, 70, 135; Plant Breeding 
in Scandinavia (Review), 35; The 
American Breeders’ Magazine, 10 

Stratosae, 82 

Struvea, 6 

Such, Mrs. G., 69 

Synechoblastus cyrtaspis, 92; flaccidus; 
92; pycnocarpum, 92; ryssoleus, 92 

Synecoccus aeruginosus, 197 

Syringia vulgaris, 35 

Syrrhopodon decolorans, 25; Hobsoni, 
25; incompletus, 25; Mohrianum, 25; 
Sartori, 25 é 


Tansley, F. D., 148 

Taubenhaus, J. J., 199 

Taxithelium planum, 30 

Taxodium distichum, 160, 162 

Taxus brevifolia, 61; canadensis, 45, 61 

Taylor, N., 18, 20, 69, 70, 131; Index 
Kewensis (Review), 37; Schaffner’s. 
Field Manual of Trees (Review), 
I10; The Salton Sea (Review), 226; 
Wilson’s A Naturalist in Western 
China (Review), 8 

Telochistes chrysopthalmus, 80; con- 
color, 85; lychneus, 82; parietinus, 82; 
polycarpus, 82 

Thallophyta, 204 

Thelephoraceae, 213 

Thompson, W. G., 112 

Thrombium epigaea, 95 

Thuidium miradoricum, 30 

Thuja plicata, 61 

Thysanophora, 137 

Tiarella, 61 

Tilia americana, 178, 183, 184 

Tiliaceae, 245 

Tithymalus campestris, 7; 
codorum, 137; Willistoni, 137 

Toninia granosa, 88 

Torrey Botanical Club, 148; Chairmen 
of Special Committees on Local Flora, 
34 

TORREYA, 129 

Trapa alabamensis, 107; bicornis, 106; 
bispinosa, 106; cuneata, 106; Cred- 
neri, 106; natans, 105, 106; micro- 
phylla, 106; wilcoxensis, 106, 107 

Trapa, Two New Tertiary Species of, 
105 

Tremellaceae, 213 

Tri- and Tetracarpellary Walnuts, 127 

Triadenum petiolatum, I51 

Trichostema dichotoma, 186; dichoto- 
mum, 188 

Trichosteleum fluviale, 31; microcar- 
pum, 31 

Trientalis americana, 43, 179 

Trilliaceae, 236 


phena- 


267 


Trillium, 61; cernuum, 179; erectum, 
179; 42 

Trypetheliaceae, 94 

Trypethelium cruentium, 94; virens, 94 

Tsuga canadensis, 178, 183, 184; hetero- 
phylla, 61; Mertensiana, 63 

Tussilago Farfara, 42 

Two Additions to the Flora of Louisiana, 
21 

Two British Columbian Notes, 45 

Two New Plants from the Tertiary 
Rocks of the West, 135 

Two New Tertiary Species of Trapa, 105 

Two Recent Works on the Marine 
Algae (Review), 4 

Typhaceae, 230 


Ueber den Einfluss des Tabakrauches 
auf der Pflanze (Review), 34 

Ulmaceae, 238 

Ulva lactuca, 98 

Umbilicaria, 88; Dilleni, 88; hirsuta, 88; 
Muhlenbergii, 88; papulosa, 88; 
pennsylvanica, 88; 170; pustulata, 88; 
pustulata papulosa, 88; vellea, 88 

Underwood Fund, 130 

Urceolaria scruposa, 91 

Urticaceae, 238 

Usnea, 139; angulata, 79; articulata, 
139; barbata, 78, 79; barbata cera- 
tina, 79; barbata dasypaoga, 79; 
barbata florida, 79; barbata hirta, 79; 
barbata plicata, 79; barbata rubigi- 
nea, 79; californica, 139; florida, 79; 
florida hirta, 79; florida rubiginea, 79; 
longissima, 79; plicata, 79, 139; pli- 
cata Huei, 79; trichodea, 79 ‘ 

Usneaceae, 78, 139 

Usneei, 78 

Ustilaginaceae, 2II 


Vacciniaceae, 248 

Vaccinium pennsylvanicum, 102, 173, 
177; vacillans, 173, 177; Vitis-Idaea, 
66 

Valeriana capitata, 66 

Valerianaceae, 251 

Van Loan, C., 129 

Van Tieghem, P. E. L., death of, 96 

Vegetation of Connecticut—III, The, 
167 

Vegetation of the Smaller Islands be- 
longing to Porto Rica, The, 164 


Verbascum Thapsus, 181 

Verbenaceae, 249 

Vernonia, 113 

Verrucaria epigaea, 95; nitida, 95 

Verrucariaceae, 95 

Vesicularia amphiloba, 31; vesicularis, 
31 

Viburnum acerifolium, 177, 179; molle, 
160; nudum, 160 

Vicia sativa, 34 

Viola, 42; Brittoniana, 4; emarginata, 3, 
4; emarginata X septemloba, 3, 4; 
pedata, 173; fimbriatula, 189; pedata 
lineariloba, 102; septemloba, 2, 4; 
villosa, 4 

Violaceae, 246 

Violets New to Southeastern Virginia, 2 

Vitaceae, 245 

Vitrea, 137 


Wager, H., The Action of Light on 
Chlorophyll (Review), 111 

Warner, C. H., Formaldehyde as an 
Oxidation Product of Chlorophyll 
Extracts (Review), III 

Watson, J. H., death of, 131 

White, O. E., 17, 130 

Whorled Leaves in Gentiana, 108 

Wieland, G. R., 96 

Wild Flowers of Spring, 164 

Wille, N., 255 

Williams, R. S. & Britton, 
Central American Mosses, 24 

Wilson, E. H., 38 

Wilson, G. W., 165 

Wilson’s A Naturalist in Western China 
(Review), 8 

Winter Changes in Weeping Willow, 31 - 

Wood, G. C., A Preliminary List of the 
Lichens found within a Radius of 
too Miles of New York City, 73 

Woodsia ilvensis, 171, 172 


135 (Ce 


Xanthium, 12, 13, 14; fruticosum, 12 

Xanthoria lychnea, 82; parietina, 82; 
polycarpa, 82 

Xylogropha parallela, 92 

Xyridaceae, 235 


Zannichelliaceae, 230 
Zizaniopsis miliacea, 151 
Zostera, 100, IOI 
Zosteraceae, 230 


The Torrey Botanical Club 


Contributors of accepted ee and reviews, who wish six 
ie gratuitous copies of the number of TORREYA in which their. papers 


of appear, will kindly notify the editor when returning proot. 


aS Reprints should be ordered, when galley proof is returned 
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: ue following Commiittees have been appointed for 1914. 


Finance Committee ‘Field Committee 
ge fee “BARNHART, ‘Chairman SERENO STETSON, Chairman 
"Miss C. C. Haynes 
Budget Committee : _ Program Committee . 
J. H. Barnuart, Chairman Mrs. E. G. Briton, Chairman 
--L. Brirton” Muss Jean BROADHURST 
OOper 22); ie: C. Sruart GacEer 
A. Howe sees PF. J, SEAVER 
W.. EVANs ee 
H. Ruspy 


aes 


Local Flora Committee 
: N.L. Brrrron, Charman: . : 
Phanerogams: = ~~ s - Cryptogams: — 


By PY Bick nei. ~~ Mrs: EG. Brirron 
AN2 LL. BRittone6. 7% PHitie DOWELL © 
CC Gorrs Shae Tracy E: Hazen’ 
K. K. Mackenzie “M. A. Howe 
Norman AL ANDOR. 3 ee WA. Mugrice. 


"Delegate to the Council of the New York Academy of Sciences : : 
2 WILLIAM MANSFIELD 


OTHER PU BLICAT IONS 


OF THE. 


TORREY BOTANICAL CLUB 


(3). BULLETIN | 


| A acnitily journal devoted to general botany, setalapdied oe 
1870. Vol. 40 published in 1913, contained 712 pages of text 


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“(2) MEMOIRS 


The MEMOIRS, established 1889, are published at Bae 
intervals. Volumes 1— 13 are now completed ; Nos. 1.and 2 of 


Vol. 14 have been ‘issued, The subscription price is fixed ate 
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b Columbia University - 


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